(Q24336919)

GOA release 2020-03-11

muscle organ development

1 reference

GOA release 2020-03-11

muscular dystrophy

1 reference

autosomal recessive limb-girdle muscular dystrophy type 2D

inferred from title

1 reference

6

0 references

Steven L Roberds

object named as

S L Roberds

2

0 references

author name string

F Piccolo

1

0 references

M Jeanpierre

3

0 references

F Leturcq

4

0 references

K Azibi

5

0 references

A Carrié

7

0 references

D Récan

8

0 references

M Chaouch

9

0 references

A Reghis

https://scigraph.springernature.com/pub.10.1038/ng0695-243

10

0 references

language of work or name

English

0 references

publication date

June 1995

0 references

published in

Nature Genetics

0 references

volume

10

0 references

page(s)

243-5

0 references

issue

2

0 references

exact match

0 references

cites work

Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038/NG0695-243

Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle

20 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-243

7 January 2021

Glycoprotein complex anchoring dystrophin to sarcolemma

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-243

7 January 2021

Membrane organization of the dystrophin-glycoprotein complex

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-243

7 January 2021

Severe childhood muscular dystrophy affecting both sexes and frequent in Tunisia

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-243

7 January 2021

Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-243

7 January 2021

Linkage analysis of families with severe childhood autosomal recessive muscular dystrophy in Morocco indicates genetic homogeneity of the disease in north Africa

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-243

7 January 2021

Genetic heterogeneity for Duchenne-like muscular dystrophy (DLMD) based on linkage and 50 DAG analysis.

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-243

7 January 2021

Selective defect of sarcoglycan complex in severe childhood autosomal recessive muscular dystrophy muscle

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-243

7 January 2021

Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q.

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-243

7 January 2021

Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-243

7 January 2021

Adhalin gene polymorphism

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-243

7 January 2021

Dystrophin in skeletal muscle. I. Western blot analysis using a monoclonal antibody

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-243

7 January 2021