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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...
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| 主要な著者: | , , , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Public Library of Science
2009
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| 主題: | |
| オンライン･アクセス: | 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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