Genetic analyses of Vietnamese patients with oculocutaneous albinism-Reference-Cited by-同舟云学术

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Genetic analyses of Vietnamese patients with oculocutaneous albinism

Published:2022-07-23 Issue:9 Volume:36 Page:
ISSN:0887-8013
Container-title:Journal of Clinical Laboratory Analysis
language:en
Short-container-title:Clinical Laboratory Analysis

Author:

Thuong Ma Thi Huyen¹²,Anh Luong Thi Lan³,Nhung Vu Phuong¹,Ngoc Tran Thi Bich¹,Lan Hoang Thu³,Phuong Doan Kim³,Ha Nguyen Hai¹²,Van Hai Nong¹²,Ton Nguyen Dang¹²^ORCID

Affiliation:

1. Institute of Genome Research (IGR) Vietnam Academy of Science and Technology (VAST) Ha Noi Vietnam

2. Graduated University of Science and Technology Vietnam Academy of Science and Technology (VAST) Ha Noi Vietnam

3. Department of Medical Biology and Genetics Hanoi Medical University Hanoi Viet Nam

Funder

National Foundation for Science and Technology Development

Publisher

Wiley

Subject

Microbiology (medical),Biochemistry (medical),Medical Laboratory Technology,Clinical Biochemistry,Public Health, Environmental and Occupational Health,Hematology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jcla.24625

Reference30 articles.

1. Mutational analysis of oculocutaneous albinism: a compact review;Kamaraj B;Biomed Res Int,2014

2. HPS11 and OCA8: Two new types of albinism associated with mutations in BLOC1S5 and DCT genes

3. OCA5,a novel locus for non-syndromic oculocutaneous albinism, maps to chromosome 4q24

4. Mutational data integration in gene-oriented files of the Hermansky-Pudlak Syndrome database

5. Hermansky-Pudlak syndrome: pigmentary and non-pigmentary defects and their pathogenesis

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