학술논문
A deep intronic variant in DNM1 in a patient with developmental and epileptic encephalopathy creates a splice acceptor site and affects only transcript variants including exon 10a
Document Type
Article
Author
Source
In: Neurogenetics . (Neurogenetics, July 2023, 24(3):171-180)
Subject
Language
English
ISSN
13646753
13646745
13646745