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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Detalles Bibliográficos
Autores principales: 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: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2777406/
https://www.ncbi.nlm.nih.gov/pubmed/19936226
http://dx.doi.org/10.1371/journal.pone.0007771

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2777406/
https://www.ncbi.nlm.nih.gov/pubmed/19936226
http://dx.doi.org/10.1371/journal.pone.0007771

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