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A Mutation in the TRPC6 Cation Channel Causes Familial Fo... | ResearchHub
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A Mutation in the TRPC6 Cation Channel Causes Familial Focal Segmental Glomerulosclerosis
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Authors
Michelle Winn
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Michelle Winn
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Michelle Winn
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Paul Rosenberg
Published
May 7, 2005
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Journal
Science
Topics
Biology
Endocrinology
Medicine
Nephrology
Molecular Biology
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DOI
10.1126/science.1106215
