دورية أكاديمية

Novel compound heterozygous mutations in OCA2 gene associated with non-syndromic oculocutaneous albinism in a Chinese Han patient: a case report

التفاصيل البيبلوغرافية
العنوان: Novel compound heterozygous mutations in OCA2 gene associated with non-syndromic oculocutaneous albinism in a Chinese Han patient: a case report
المؤلفون: Wang, HairongAff1, Wan, YangAff2, Yang, YunAff1, Aff3, Li, HaoAff1, Mao, LiangweiAff1, Aff4, Gao, ShuyangAff5, Xu, JingjingAff6, Wang, JingAff6
المصدر: BMC Medical Genetics. 20(1)
قاعدة البيانات: Springer Nature Journals
الوصف
تدمد:14712350
DOI:10.1186/s12881-019-0850-7