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Mutational Analysis of the TYR and OCA2 Genes in Four Chinese Families with Oculocutaneous Albinism.

机译：中国四个家庭眼皮肤白化病家系TYR和OCa2基因的突变分析。

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Yun Wang; Zhi Wang; Mengping Chen; Ning Fan; Jie Yang; Lu Liu; Ying Wang; Xuyang Liu;
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1. Mutational Analysis of TYR , OCA2, and SLC45A2 Genes in Chinese Families with Oculocutaneous Albinism [J] . Ye Lin, Xihui Chen, Ying Yang, Molecular Genetics & Genomic Medicine . 2019,第7期

机译：血管皮内常杂化的中国家庭中TYR，OCA2和SLC45A2基因的突变分析
2. High-resolution array-CGH in patients with oculocutaneous albinism identifies new deletions of the TYR, OCA2, and SLC45A2 genes and a complex rearrangement of the OCA2 gene [J] . Fanny Morice-Picard, Eulalie Lasseaux, Dorothée Cailley, Pigment cell & melanoma research . 2014,第1期

机译：眼皮肤白化病患者的高分辨率阵列CGH可以识别TYR，OCA2和SLC45A2基因的新缺失以及OCA2基因的复杂重排
3. Genetic analysis of oculocutaneous albinism type 1 (OCA1) inIndian families: two novel frameshift mutations in the TYR gene [J] . Molecular vision . 2004,第2004期

机译：眼科白化病1型（OCA1）在印度家庭的遗传分析：TYR基因中的两个新的移码突变
4. A novel mutation of the PTCH1 gene activates the Shh/Gli signaling pathway in a Chinese family with nevoid basal cell carcinoma syndrome [C] . Tingting Zhang, Mingjie Chen, Yan Lü, Academic Committee Conference of Shanghai key lab of stomatology . 2011

机译：PTCH1基因的新型突变激活了中国患有避免基底细胞癌综合征的中国家庭的Shh / Gli信号通路
5. DNA mutation analysis of voltage-gated ion channel genes in two families with sick sinus syndrome and atrial fibrillation/AV nodal reentry tachycardia. [D] . Oh, Frances. 2010

机译：两个病态窦房结综合征和房颤/房室结折返性心动过速患者的电压门控离子通道基因的DNA突变分析。
6. Mutational Analysis of TYR OCA2 and SLC45A2 Genes in Chinese Families with Oculocutaneous Albinism [O] . Ye Lin, Xihui Chen, Ying Yang, 2019

机译：眼皮肤白化病家庭中TYROCA2和SLC45A2基因的突变分析
7. Mutational Analysis of TYR Gene Causing Oculocutaneous Albinism in Families from District Peshawar [O] . Farhan Ullah 2019

机译：TYR基因的突变分析，导致分区近叶川家庭血管皮肤仿生

Mutational Analysis of the TYR and OCA2 Genes in Four Chinese Families with Oculocutaneous Albinism.

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