Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of -dystroglycan
Year: 2003
Type: article
Study design: Observational Study
Source: Human Molecular Genetics
DOI: 10.1093/hmg/ddg307
Author: C. Longman
Institution: Imperial College London
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2156863768
