Genetic analyses of Vietnamese patients with oculocutaneous albinism

BACKGROUND: Oculocutaneous albinism (OCA) is an autosomal recessive disease with hypopigmentation in skin, hair, and eyes, causing by the complete absence or reduction of melanin in melanocytes. Many types of OCA were observed based on the mutation in different causing genes relating to albinism. OC...

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Detalles Bibliográficos
Autores principales: Thuong, Ma Thi Huyen, Anh, Luong Thi Lan, Nhung, Vu Phuong, Ngoc, Tran Thi Bich, Lan, Hoang Thu, Phuong, Doan Kim, Ha, Nguyen Hai, Van Hai, Nong, Ton, Nguyen Dang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9459276/
https://www.ncbi.nlm.nih.gov/pubmed/35870188
http://dx.doi.org/10.1002/jcla.24625

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9459276/
https://www.ncbi.nlm.nih.gov/pubmed/35870188
http://dx.doi.org/10.1002/jcla.24625

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