Identifying putative promoter regions of Hermansky-Pudlak syndrome genes by means of phylogenetic footprinting

HPS is an autosomal recessive disorder characterized by oculocutaneous albinism and prolonged bleeding. Eight human genes are described resulting in the HPS subtypes 1–8. Certain HPS proteins combine to form Biogenesis of Lysosome-related Organelles Complexes (BLOCs), thought to function in the form...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Stanescu, H., Wolfsberg, T.G., Moreland, R.T., Ayub, M.H., Erickson, E., Westbroek, W., Huizing, M., Gahl, W.A., Helip-Wooley, A.
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
Assuntos:
Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2730976/
https://ncbi.nlm.nih.gov/pubmed/19523149
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1469-1809.2009.00525.x
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados