학술논문
A novel de novo frameshift deletion in EHMT1 in a patient with Kleefstra Syndrome results in decreased H3K9 dimethylation
Document Type
Article
Author
Source
In: Molecular Genetics and Genomic Medicine . (Molecular Genetics and Genomic Medicine, March 2017, 5(2):141-146)
Subject
Language
English
ISSN
23249269