학술논문
Variants of human CLDN9 cause mild to profound hearing loss
Document Type
Article
Author
Ramzan, M.; Basheer, R.; Munir, Z.; Idrees, H.; Salman, M.; Naz, S.; Belyantseva, I.A.; Fenollar-Ferrer, C.; Tona, R.; Yousaf, R.; Imtiaz, A.; Faridi, R.; Friedman, T.B.; Philippe, C.; Vitobello, A.; Nambot, S.; Moutton, S.; Nakano, Y.; Banfi, B.; Kartti, S.; Zarrik, O.; Ibrahimi, A.; Witmer, P.D.; Sobreria, N.
Source
In: Human Mutation . (Human Mutation, October 2021, 42(10):1321-1335)
Subject
Language
English
ISSN
10981004
10597794
10597794