A Novel De Novo GATA Binding Protein 3 Mutation in a Turkish Boy with Hypoparathyroidism, Deafness, and Renal Dysplasia Syndrome.
| Autor: | Yeşiltepe Mutlu, Gül1 gulyesiltepe@gmail.com, Kırmızıbekmez, Heves1, Nakamura, Akie2, Fukami, Maki2, Hatun, Şükrü3 |
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| Zdroj: | Journal of Clinical Research in Pediatric Endocrinology. Dec2015, Vol. 7 Issue 4, p344-348. 5p. |
| Databáze: | Academic Search Ultimate |
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