Genetic Heterogeneity of KID Syndrome: Identification of a Cx30 Gene (GJB6) Mutation in a Patient with KID Syndrome and Congenital Atrichia
| Autor: | Jan, Amy Y. *, Amin, Shivan, Ratajczak, Paulina, Richard, Gabriele *, Sybert, Virginia P. |
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| Zdroj: | In Journal of Investigative Dermatology May 2004 122(5):1108-1113 |
| Databáze: | ScienceDirect |
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