Oculocutaneous albinism and bleeding diathesis due to a novel deletion in the HPS3 gene

Hermansky–Pudlak syndrome (HPS) is a group of rare autosomal recessive disorders characterized by oculocutaneous albinism (OCA) and bleeding diathesis. To date, 11 HPS types have been reported (HPS-1 to HPS-11), each defined by disease-causing variants in specific genes. Variants in the HPS1 gene we...

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Detalles Bibliográficos
Autores principales: Marek-Yagel, Dina, Abudi-Sinreich, Shachar, Macarov, Michal, Veber, Alvit, Shalva, Nechama, Philosoph, Amit Mary, Pode-Shakked, Ben, Malicdan, May Christine V., Anikster, Yair
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9420964/
https://www.ncbi.nlm.nih.gov/pubmed/36046236
http://dx.doi.org/10.3389/fgene.2022.936064

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9420964/
https://www.ncbi.nlm.nih.gov/pubmed/36046236
http://dx.doi.org/10.3389/fgene.2022.936064

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