Whole‐genome sequencing revealed a novel long‐range deletion mutation spanning GNAS in familial pseudohypoparathyroidism.

Autor: Fei, Yangfan1 (AUTHOR) feiyangfan_mmph@163.com, Liu, Lv1 (AUTHOR), Wu, Lixia1 (AUTHOR), Wang, Ou2 (AUTHOR), Xing, Xiaoping2 (AUTHOR), Li, Aiping1 (AUTHOR), Huang, Lingyi1 (AUTHOR)
Zdroj: Molecular Genetics & Genomic Medicine. May2023, Vol. 11 Issue 5, p1-10. 10p.
Databáze: Academic Search Ultimate
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