| Literature DB >> 507050 |
Abstract
Congenital universal muscular hypoplasia has been confused with similar diseases in the past. Evidence presented in this paper distinguishes this disorder from other phenotypically similar ones and indicates that it is inherited as an autosomal recessive disorder.Entities:
Mesh：
Year: 1979 PMID： 507050 PMCID： PMC1685907
Source DB: PubMed Journal: Am J Hum Genet ISSN： 0002-9297 Impact factor: 11.025