دورية أكاديمية
Novel compound heterozygous mutations in OCA2 gene associated with non-syndromic oculocutaneous albinism in a Chinese Han patient: a case report
العنوان: | Novel compound heterozygous mutations in OCA2 gene associated with non-syndromic oculocutaneous albinism in a Chinese Han patient: a case report |
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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 |
تدمد: | 14712350 |
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DOI: | 10.1186/s12881-019-0850-7 |