Novel compound heterozygous mutations in OCA2 gene were identified in a Chinese family with oculocutaneous albinism.

Autor: Jiang, Beilei1 (AUTHOR), Zhang, Hua1 (AUTHOR), Kan, Yuling2 (AUTHOR), Gao, Xueping3 (AUTHOR), Du, Zhaoli3 (AUTHOR), Liu, Quan1 (AUTHOR) 534520384@qq.com
Zdroj: Molecular Genetics & Genomic Medicine. Jan2024, Vol. 12 Issue 1, p1-11. 11p.
Databáze: Academic Search Ultimate
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