Hearing Loss is an Early Consequence of Npc1 Gene Deletion in the Mouse Model of Niemann–Pick Disease, Type C

Niemann–Pick disease, type C1 (NPC1) is a rare lysosomal lipidosis that is most often the result of biallelic mutations in NPC1, and is characterized by a fatal neurological degeneration. The pathophysiology is complex, and the natural history of the disease is poorly understood. Recent findings fro...

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Detalhes bibliográficos
Main Authors: King, Kelly A., Gordon-Salant, Sandra, Pawlowski, Karen S., Taylor, Anna M., Griffith, Andrew J., Houser, Ari, Kurima, Kiyoto, Wassif, Christopher A., Wright, Charles G., Porter, Forbes D., Repa, Joyce J., Brewer, Carmen C.
Formato: Artigo
Idioma:Inglês
Publicado em: Springer US 2014
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4141427/
https://ncbi.nlm.nih.gov/pubmed/24839095
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10162-014-0459-7
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