A benign allelic form of laminin alpha 2 chain deficient muscular dystrophy (Q73252994)

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scientific article published on 01 April 1997

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Language	Label	Description	Also known as
English	A benign allelic form of laminin alpha 2 chain deficient muscular dystrophy	scientific article published on 01 April 1997

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9113020

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9113020%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

title

A benign allelic form of laminin alpha 2 chain deficient muscular dystrophy (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9113020

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9113020%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

main subject

muscular dystrophy

1 reference

based on heuristic

inferred from title

author name string

Y K Hayashi

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9113020

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9113020%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

T Ishihara

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9113020

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9113020%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

K Domen

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9113020

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9113020%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

H Hori

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9113020

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9113020%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

K Arahata

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9113020

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9113020%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

language of work or name

English

0 references

publication date

1 April 1997

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9113020

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9113020%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

published in

The Lancet

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9113020

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9113020%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

volume

349

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9113020

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9113020%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

issue

9059

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9113020

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9113020%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

page(s)

1147

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9113020

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9113020%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

cites work

Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2963023-1

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2963023-1

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Refinement of the laminin alpha2 chain locus to human chromosome 6q2 in severe and mild merosin deficient congenital muscular dystrophy

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2963023-1

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1016/S0140-6736(05)63023-1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9113020

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9113020%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

PubMed publication ID

9113020

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9113020

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9113020%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

 

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