A Novel TRPC6 Mutation That Causes Childhood FSGS

BACKGROUND: TRPC6, encoding a member of the transient receptor potential (TRP) superfamily of ion channels, is a calcium-permeable cation channel, which mediates capacitive calcium entry into the cell. Until today, seven different mutations in TRPC6 have been identified as a cause of autosomal-domin...

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Detalhes bibliográficos
Main Authors: Heeringa, Saskia F., Möller, Clemens C., Du, Jianyang, Yue, Lixia, Hinkes, Bernward, Chernin, Gil, Vlangos, Christopher N., Hoyer, Peter F., Reiser, Jochen, Hildebrandt, Friedhelm
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2009
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2777406/
https://ncbi.nlm.nih.gov/pubmed/19936226
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0007771
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