| Literature DB >> 15941405 |
Marta Hoffman-Sommer1, Marcin Grynberg, Roza Kucharczyk, Joanna Rytka.
Abstract
Hermansky-Pudlak syndrome (HPS) is a rare disorder caused by malfunctions of lysosomes and specialized lysosome-related organelles, resulting primarily in oculocutaneous albinism and bleeding diathesis. The majority of the HPS genes have been described as novel, but herein we report the identification of a conserved protein family which includes human HPS4, as well as distant homologs for other HPS genes. Our results suggest that the cellular machinery involved in the HPS syndrome is ancient.Entities:
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Year: 2005 PMID: 15941405 DOI: 10.1111/j.1600-0854.2005.00301.x
Source DB: PubMed Journal: Traffic ISSN: 1398-9219 Impact factor: 6.215