ATP8B1 is essential for maintaining normal hearing

ATP8B1 deficiency is caused by autosomal recessive mutations in ATP8B1, which encodes the putative phospatidylserine flippase ATP8B1 (formerly called FIC1). ATP8B1 deficiency is primarily characterized by cholestasis, but extrahepatic symptoms are also found. Because patients sometimes report reduce...

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Detalhes bibliográficos
Main Authors: Stapelbroek, Janneke M., Peters, Theo A., van Beurden, Denis H. A., Curfs, Jo H. A. J., Joosten, Anneke, Beynon, Andy J., van Leeuwen, Bibian M., van der Velden, Lieke M., Bull, Laura, Oude Elferink, Ronald P., van Zanten, Bert A., Klomp, Leo W. J., Houwen, Roderick H. J.
Formato: Artigo
Idioma:Inglês
Publicado em: National Academy of Sciences 2009
Assuntos:
Biological Sciences
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2700994/
https://ncbi.nlm.nih.gov/pubmed/19478059
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0807919106
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