Duplication of proteolipid protein gene: a possible major cause of Pelizaeus-Merzbacher disease (Q50924723)

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scientific article published in September 1997

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Language	Label	Description	Also known as
English	Duplication of proteolipid protein gene: a possible major cause of Pelizaeus-Merzbacher disease	scientific article published in September 1997

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scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9367291

retrieved

25 March 2018

reference URL

http://europepmc.org/abstract/MED/9367291

title

Duplication of proteolipid protein gene: a possible major cause of Pelizaeus-Merzbacher disease (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9367291

retrieved

25 March 2018

reference URL

http://europepmc.org/abstract/MED/9367291

author

Wuh-liang Hwu

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9367291

retrieved

25 March 2018

reference URL

http://europepmc.org/abstract/MED/9367291

Wang-Tso Lee

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9367291

retrieved

25 March 2018

reference URL

http://europepmc.org/abstract/MED/9367291

author name string

Wang PJ

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9367291

retrieved

25 March 2018

reference URL

http://europepmc.org/abstract/MED/9367291

Wang TR

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9367291

retrieved

25 March 2018

reference URL

http://europepmc.org/abstract/MED/9367291

Shen YZ

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9367291

retrieved

25 March 2018

reference URL

http://europepmc.org/abstract/MED/9367291

publication date

1 September 1997

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9367291

retrieved

25 March 2018

reference URL

http://europepmc.org/abstract/MED/9367291

published in

Pediatric Neurology

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9367291

retrieved

25 March 2018

reference URL

http://europepmc.org/abstract/MED/9367291

volume

17

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9367291

retrieved

25 March 2018

reference URL

http://europepmc.org/abstract/MED/9367291

issue

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9367291

retrieved

25 March 2018

reference URL

http://europepmc.org/abstract/MED/9367291

page(s)

125-128

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9367291

retrieved

25 March 2018

reference URL

http://europepmc.org/abstract/MED/9367291

cites work

An interstitial duplication of the X chromosome in a male allows physical fine mapping of probes from the Xq13-q22 region

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900088-X

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

The gene encoding for the major brain proteolipid (PLP) maps on the q-22 band of the human X chromosome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900088-X

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

DM20 mRNA splice product of the myelin proteolipid protein gene is expressed in the murine heart

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900088-X

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A new mutation in the proteolipid protein (PLP) gene in a German family with pelizaeus-merzbacher disease

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900088-X

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

In-frame deletion in the proteolipid protein gene of a family with Pelizaeus-Merzbacher disease

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900088-X

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Proteolipid protein gene dosage effect in Pelizaeus-Merzbacher disease

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900088-X

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Overexpression of DM20 messenger RNA in two brothers with Pelizaeus-Merzbacher disease

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900088-X

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Neurophysiologic studies and MRI in Pelizaeus-Merzbacher disease: comparison of classic and connatal forms

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Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900088-X

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Glucose-6-phosphatase gene G327A mutation is common in Chinese patients with glycogen storage disease type Ia

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900088-X

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Premature arrest of myelin formation in transgenic mice with increased proteolipid protein gene dosage

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900088-X

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Glial cell degeneration and hypomyelination caused by overexpression of myelin proteolipid protein gene

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900088-X

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900088-X

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP)

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900088-X

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1016/S0887-8994(97)00088-X

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9367291

retrieved

25 March 2018

reference URL

http://europepmc.org/abstract/MED/9367291

PubMed publication ID

9367291

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9367291

retrieved

25 March 2018

reference URL

http://europepmc.org/abstract/MED/9367291

 

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