(Q71791406)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7580243%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

title

Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal muscle (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7580243%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

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

1 reference

https://api.crossref.org/works/10.1016/0960-8966(94)00069-L

congenital muscular dystrophy

21 May 2024

main subject

1 reference

1 reference

J. Philpot

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7580243

21 May 2024

C. Sewry

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7580243

21 May 2024

J. Pennock

0 references

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7580243

21 May 2024

publication date

1 July 1995

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7580243%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

published in

Neuromuscular Disorders

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7580243%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

volume

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7580243%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7580243%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

page(s)

301-305

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7580243%20AND%20SRC:MED&resulttype=core&format=json

Familial concordance of brain magnetic resonance imaging changes in congenital muscular dystrophy

21 October 2019

cites work

5

1 reference

https://api.crossref.org/works/10.1016/0960-8966(94)00069-L

Congenital muscular dystrophy with merosin deficiency

21 May 2024

6

1 reference

https://api.crossref.org/works/10.1016/0960-8966(94)00069-L

Laminin variants: why, where and when?

21 May 2024

8

1 reference

https://api.crossref.org/works/10.1016/0960-8966(94)00069-L

Human laminin M chain (merosin): complete primary structure, chromosomal assignment, and expression of the M and A chain in human fetal tissues

21 May 2024

9

1 reference

https://api.crossref.org/works/10.1016/0960-8966(94)00069-L

Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping

21 May 2024

10

1 reference

https://api.crossref.org/works/10.1016/0960-8966(94)00069-L

21 May 2024

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7580243%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

1 reference