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A novel TRPC6 mutation in a family with podocytopathy and clinical variability

Creator: Mottl, Amy K., Lu, Mei, Fine, Catherine A., Weck, Karen E.

Abstract Background Mutation in several podocyte-specific genes have been noted to result in phenotypic heterogeneity. Herein, we report a novel, autosomal dominant TRPC6 mutation in a family with disease ranging from asymptomatic minimal change (more)

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12882_2012_article_532.pdf

Collection: BioMed Central

Date Deposited: 2016-07-15

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Figure 2 Sequence analysis of the novel TRPC6 mutation found in 3 family members.

Collection: BioMed Central

Date Deposited: 2016-07-15

Date Created: 2016-07-15

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