Rhizomelic Chondrodysplasia Punctata Type 1 Caused by a Novel Mutation in the PEX7 Gene.
| Autor: | Çim, Abdullah1 drabdullahcim@yahoo.com, Coşkun, Salih1, Görükmez, Orhan2, Yüksel, Hatice3, Uluca, Ünal4, Di Pietro, Erminia5, Plourde, François5, Braverman, Nancy Elise5 |
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| Zdroj: | Journal of Clinical Research in Pediatric Endocrinology. Mar2015, Vol. 7 Issue 1, p69-72. 4p. |
| Databáze: | Academic Search Ultimate |
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