A novel X-linked gene, G4.5. is responsible for Barth syndrome (Q28278751)

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English	A novel X-linked gene, G4.5. is responsible for Barth syndrome	scientific article

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instance of

scholarly article

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title

A novel X-linked gene, G4.5. is responsible for Barth syndrome (English)

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main subject

Barth syndrome

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based on heuristic

inferred from title

author

Patrizia D'Adamo

object named as

P D'Adamo

series ordinal

2

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Silvia Bione

object named as

S Bione

series ordinal

1

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author name string

E Maestrini

series ordinal

3

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A K Gedeon

series ordinal

4

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P A Bolhuis

series ordinal

5

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D Toniolo

series ordinal

6

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language of work or name

English

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publication date

April 1996

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published in

Nature Genetics

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volume

12

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issue

4

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page(s)

385-9

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cites work

An analysis of vertebrate mRNA sequences: intimations of translational control

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038/NG0496-385

retrieved

21 April 2017

An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0496-385

retrieved

21 January 2018

24 Rapid amplification of complementary DNA ends for generation of full-length complementary DNAs: Thermal race

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0496-385

retrieved

21 January 2018

X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0496-385

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Barth syndrome: clinical features and confirmation of gene localisation to distal Xq28.

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0496-385

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Transcriptional organization of a 450-kb region of the human X chromosome in Xq28

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0496-385

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0496-385

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of new mutations in the Emery-Dreifuss muscular dystrophy gene and evidence for genetic heterogeneity of the disease

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0496-385

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Multiple mechanisms of protein insertion into and across membranes.

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0496-385

retrieved

7 January 2021

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Identifiers

DOI

10.1038/NG0496-385

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2722510

Fatcat ID

release_ksg5rlicyffwhm6ostq6zni34m

1 reference

stated in

Fatcat

reference URL

https://api.fatcat.wiki/v0/release/ksg5rlicyffwhm6ostq6zni34m

retrieved

24 November 2022

based on heuristic

mapped directly with Wikidata item

OpenCitations bibliographic resource ID

2722510

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2722510

PubMed publication ID

8630491

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2722510

ResearchGate publication ID

14569052

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