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A new type of oculocutaneous albinism with a novel OCA2 mutation
Oculocutaneous albinism (OCA) is a group of rare genetically heterogeneous disorders, characterized by hypopigmentation of the eyes, skin, and hair, which result in ocular abnormalities and a risk of developing skin cancer. Currently, there is no ophthalmologic procedure or drug that prevents the cl...
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| Publicado no: | Yeungnam Univ J Med |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Yeungnam University College of Medicine
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8016618/ https://ncbi.nlm.nih.gov/pubmed/32741191 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12701/yujm.2020.00339 |
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