Gül YEŞİLTEPE MUTLU, Heves KIRMIZIBEKMEZ, Akie NAKAMURA, Maki FUKAMİ, ŞÜKRÜ HATUN

A Novel De Novo GATA Binding Protein 3 Mutation in a Turkish Boy with Hypoparathyroidism, Deafness, andRenal Dysplasia Syndrome

Journal of Clinical Research in Pediatric Endocrinology

2015-Cilt: 7 - Sayı: 4

344-348

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