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Identification of Novel Compound Heterozygous MYO15A Mutations in Two Chinese Families with Autosomal Recessive Nonsyndromic Hearing Loss

机译：两种中国家庭的新化合物杂合酶肌瘤突变鉴定常染色体隐性非合成瘤性听力损失

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Xiao-Hui Wang; Le Xie; Sen Chen; Kai Xu; Xue Bai; Yuan Jin; Yue Qiu; Xiao-Zhou Liu; Yu Sun; Wei-Jia Kong;
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1. Identification of Novel Compound Heterozygous MYO15A Mutations in Two Chinese Families with Autosomal Recessive Nonsyndromic Hearing Loss [J] . Xiao-Hui Wang, Wei-Jia Kong, Le Xie, Journal of Neural Transplantation and Plasticity: Neural Plasticity . 2021,第a期

机译：两种中国家庭的新化合物杂合酶肌瘤突变鉴定常染色体隐性非合成瘤性听力损失
2. Compound Heterozygous Mutations in TMC1 and MYO15A Are Associated with Autosomal Recessive Nonsyndromic Hearing Loss in Two Chinese Han Families [J] . Pengcheng Xu, Jun Xu, Hu Peng, Journal of Neural Transplantation and Plasticity: Neural Plasticity . 2020,第Supplementa1期

机译：TMC1和MyO15A中的化合物杂合酶突变与两家中国汉族家庭中的常染色体隐性非合成型听力损失有关
3. Three MYO15A Mutations Identified in One Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss [J] . Fengguo Zhang, Lei Xu, Yun Xiao, Journal of Neural Transplantation and Plasticity: Neural Plasticity . 2018,第1期

机译：在一个常染色体隐性非综合征性听力损失中国家庭中鉴定出三个MYO15A突变
4. Identification of a Novel Compound Heterozygous Variant in NBAS Causing Bone Fragility by the Type of Osteogenesis Imperfecta [C] . D. A. Petukhova, E. E. Gurinova, A. L. Sukhomyasova, International Symposium on Bioinformatics Research and Applications . 2020

机译：通过成骨不全症类型鉴定导致骨骼脆弱的NBAS中的新型复合杂合变体
5. Investigation of daily four month sildenafil administration on heterozygous carriers of a phosphodiesterase 6 mutation in a canine model of autosomal recessive retinitis pigmentosa. [D] . Pierce, Kenneth E., Jr. 2011

机译：在常染色体隐性遗传性视网膜炎的犬模型中，每天四个月西地那非对磷酸二酯酶6突变的杂合子载体给药的研究。
6. Identification of a Novel MYO15A Mutation in a Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss [O] . Hong Xia, Xiangjun Huang, Yi Guo, -1

机译：常染色体隐性非综合征性听力损失的中国家庭中新型MYO15A突变的鉴定。
7. Identification of a Novel MYO15A Mutation in a Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss. [O] . Hong Xia, Xiangjun Huang, Yi Guo, 2015

机译：鉴定具有常染色体隐性非综合征性听力损失的中国家庭中的mYO15a突变。

Identification of Novel Compound Heterozygous MYO15A Mutations in Two Chinese Families with Autosomal Recessive Nonsyndromic Hearing Loss

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