학술논문
Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory function
Document Type
Article
Author
Lin, S.-J.; Huang, K.; Petree, C.; Varshney, G.K.; Vona, B.; Schnapp, L.; Haaf, T.; Porter, H.M.; Shur, N.; Izadi, M.; Ali, T.A.; Pourkarimi, E.; Lacassie, Y.; Rosenfeld, J.A.; Liu, P.; Khan, S.; Muhammad, N.; Khan, S.A.; Muhammad, N.; Haymon, M.-L.; Rüschendorf, F.; Kong, I.-K.; Chorich, L.; Layman, L.; Kim, H.-G.
Source
In: Human Mutation . (Human Mutation, October 2022, 43(10):1472-1489)
Subject
Language
English
ISSN
10981004
10597794
10597794