학술논문
Recurrent missense variant identified in two unrelated families with MPZL2-related hearing loss, expanding the variant spectrum associated with DFNB111
Document Type
Article
Author
Source
In: American Journal of Medical Genetics, Part A . (American Journal of Medical Genetics, Part A, May 2024, 194(5))
Subject
Language
English
ISSN
15524833
15524825
15524825