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Loss-of-Function SOX10 Mutation in a Patient with Kallmann Syndrome, Hearing Loss, and Iris Hypopigmentation
Suzuki, Erina, Izumi, Yoko, Chiba, Yuta, Horikawa, Reiko, Matsubara, Yoichi, Tanaka, Mamoru, Ogata, Tsutomu, Fukami, Maki, Naiki, YasuhiroLangue:
english
Journal:
Hormone Research in Paediatrics
DOI:
10.1159/000436965
Date:
July, 2015
Fichier:
PDF, 198 KB
english, 2015