학술논문
Transcriptome sequencing identifies a noncoding, deep intronic variant in CLCN7 causing autosomal recessive osteopetrosis
Document Type
Article
Author
Source
In: Molecular Genetics and Genomic Medicine . (Molecular Genetics and Genomic Medicine, 1 October 2020, 8(10))
Subject
Language
English
ISSN
23249269