Novel Mutations in FKBP10 and PLOD2 Cause Rare Bruck Syndrome in Chinese Patients.
| Autor: | Zhou, Peiran1, Liu, Yi1, Lv, Fang1, Nie, Min1, Jiang, Yan1, Wang, Ou1, Xia, Weibo1, Xing, Xiaoping1, Li, Mei1 limeilzh@sina.com |
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| Zdroj: | PLoS ONE. Sep2014, Vol. 9 Issue 9, p1-8. 8p. |
| Databáze: | Academic Search Ultimate |
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