Loss-of-Function SOX10 Mutation in a Patient with Kallmann Syndrome, Hearing Loss, and Iris Hypopigmentation

Publisher： Karger

E-ISSN： 1663-2826|84|3|212-216

ISSN： 1663-2818

Source： Hormone Research in Paediatrics, Vol.84, Iss.3, 2015-07, pp. : 212-216

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