Mutational Analysis of TYR , OCA2, and SLC45A2 Genes in Chinese Families with Oculocutaneous Albinism-Reference-Cited by-同舟云学术

Mutational Analysis of TYR , OCA2, and SLC45A2 Genes in Chinese Families with Oculocutaneous Albinism

Published:2019-06-14 Issue:7 Volume:7 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Lin Ye¹,Chen Xihui²^ORCID,Yang Ying³,Che Fengyu³,Zhang Sijia²,Yuan Lijuan²⁴,Wu Yuanming²

Affiliation:

1. The General Hospital of the People's Liberation Army Beijing P.R. China

2. Department of Biochemistry and Molecular Biology Center for DNA Typing, Air Force Medical University Xi'an Shaanxi P.R. China

3. Shaanxi Institute of Pediatric Diseases, Xi’an Children’s Hospital Xi’an Shaanxi P.R. China

4. Department of General Surgery Tangdu Hospital, Air Force Medical University Xi’an Shaanxi P.R. China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.687

Reference42 articles.

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4. Mutations in the gene encoding B, a novel transporter protein, reduce melanin content in medaka

5. Mutations of the tyrosinase gene in patients with oculocutaneous albinism from various ethnic groups in Israel;Gershoni‐Baruch R.;American Journal of Human Genetics,1994

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