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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...
Những tác giả chính: | , , , , , , , , , |
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Định dạng: | Texto |
Ngôn ngữ: | English |
Được phát hành: |
Public Library of Science
2009
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Những chủ đề: | |
Truy cập trực tuyến: | 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 |