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A novel TRPC6 mutation that causes childhood FSGS.
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A novel TRPC6 mutation that causes childhood FSGS.
A novel TRPC6 mutation that causes childhood FSGS. PLoS One. 2009 Nov 10; 4(11):e7771.
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PubMed
subject areas
Adolescent
Adult
Aged
Child
Child, Preschool
Cohort Studies
Family Health
Female
Gene Expression Regulation
Genes, Dominant
Glomerulosclerosis, Focal Segmental
Humans
Infant
Male
Middle Aged
Mutation
TRPC Cation Channels
TRPC6 Cation Channel