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TMTC2 variant associated with sensorineural hearing loss and auditory neuropathy spectrum disorder in a family dyad
Guillen-Ahlers, Hector, Erbe, Christy B., Chevalier, Frédéric D., Montoya, Maria J., Zimmerman, Kip D., Langefeld, Carl D., Olivier, Michael, Runge, Christina L.Language:
english
Journal:
Molecular Genetics & Genomic Medicine
DOI:
10.1002/mgg3.397
Date:
April, 2018
File:
PDF, 758 KB
english, 2018