학술논문
Identification of Biallelic dystrophin gene variants during maternal carrier testing for Becker muscular dystrophy and review of the DMD exon 49–51 deletion phenotype
Document Type
Article
Author
Source
In: Molecular Genetics and Genomic Medicine . (Molecular Genetics and Genomic Medicine, January 2023, 11(1))
Subject
Language
English
ISSN
23249269