New molecular mechanism for Ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype

Subjects

Subjects :

Muscular dystrophy -- Research
Biological sciences

Details

Language :

English

ISSN :

00029297

Volume :

73

Issue :

2

Database :

Gale General OneFile

Journal :

American Journal of Human Genetics

Publication Type :

Academic Journal

Accession number :

edsgcl.106699397