In vitro disease modeling of oculocutaneous albinism type 1 and 2 using human induced pluripotent stem cell-derived retinal pigment epithelium

Oculocutaneous albinism (OCA) encompasses a set of autosomal recessive genetic conditions that affect pigmentation in the eye, skin, and hair. OCA patients display reduced best-corrected visual acuity, reduced to absent ocular pigmentation, abnormalities in fovea development, and/or abnormal decussa...

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Detalles Bibliográficos
Autores principales: George, Aman, Sharma, Ruchi, Pfister, Tyler, Abu-Asab, Mones, Hotaling, Nathan, Bose, Devika, DeYoung, Charles, Chang, Justin, Adams, David R., Cogliati, Tiziana, Bharti, Kapil, Brooks, Brian P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Resource
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8758966/
https://www.ncbi.nlm.nih.gov/pubmed/35021041
http://dx.doi.org/10.1016/j.stemcr.2021.11.016

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8758966/
https://www.ncbi.nlm.nih.gov/pubmed/35021041
http://dx.doi.org/10.1016/j.stemcr.2021.11.016

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