Assignment of a Form of Congenital Muscular Dystrophy with Secondary Merosin Deficiency to Chromosome 1q42

We have previously reported an autosomal recessive form of congenital muscular dystrophy, characterized by proximal girdle weakness, generalized muscle hypertrophy, rigidity of the spine, and contractures of the tendo Achilles, in a consanguineous family from the United Arab Emirates. Early respirat...

Full description

Saved in:
Bibliographic Details
Main Authors: Brockington, Martin, Sewry, Caroline A., Herrmann, Ralf, Naom, Isam, Dearlove, Andrew, Rhodes, Michael, Topaloglu, Haluk, Dubowitz, Victor, Voit, Thomas, Muntoni, Francesco
Format: Artigo
Language:Inglês
Published: The American Society of Human Genetics 2000
Subjects:
Articles
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC1288095/
https://ncbi.nlm.nih.gov/pubmed/10677302
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items