BLOC-3 Mutated in Hermansky-Pudlak Syndrome Is a Rab32/38 Guanine Nucleotide Exchange Factor

Hermansky-Pudlak syndrome (HPS) is a human disease characterized by partial loss of pigmentation and impaired blood clotting [1–3]. These symptoms are caused by defects in the biogenesis of melanosomes and platelet dense granules, often referred to as lysosome-related organelles [2]. Genes mutated i...

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Detalles Bibliográficos
Autores principales: Gerondopoulos, Andreas, Langemeyer, Lars, Liang, Jin-Rui, Linford, Andrea, Barr, Francis A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2012
Materias:
Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3502862/
https://www.ncbi.nlm.nih.gov/pubmed/23084991
http://dx.doi.org/10.1016/j.cub.2012.09.020

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3502862/
https://www.ncbi.nlm.nih.gov/pubmed/23084991
http://dx.doi.org/10.1016/j.cub.2012.09.020

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