A Novel TRPC6 Mutation That Causes Childhood FSGS

• Saskia F. Heeringa,

  Affiliation Departments of Pediatrics and of Human Genetics, University of Michigan, Ann Arbor, Michigan, United States of America

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• Clemens C. Möller,

  Affiliation Department of Medicine, Division of Nephrology and Hypertension, Leonard Miller School of Medicine, University of Miami, Miami, Florida, United States of America

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• Jianyang Du,

  Affiliation Department of Cell Biology, University of Connecticut Health Center, Farmington, Connecticut, United States of America

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• Lixia Yue,

  Affiliation Department of Cell Biology, University of Connecticut Health Center, Farmington, Connecticut, United States of America

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• Bernward Hinkes,

  Affiliation Departments of Pediatrics and of Human Genetics, University of Michigan, Ann Arbor, Michigan, United States of America

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• Gil Chernin,

  Affiliation Departments of Pediatrics and of Human Genetics, University of Michigan, Ann Arbor, Michigan, United States of America

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• Christopher N. Vlangos,

  Affiliation Departments of Pediatrics and of Human Genetics, University of Michigan, Ann Arbor, Michigan, United States of America

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• Peter F. Hoyer,

  Affiliation Klinik für Pädiatrische Nephrologie, Universitäts-Kinderklinik Essen, Essen, Germany

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• Jochen Reiser,

  Affiliation Department of Medicine, Division of Nephrology and Hypertension, Leonard Miller School of Medicine, University of Miami, Miami, Florida, United States of America

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• Friedhelm Hildebrandt

  * E-mail: fhilde@umich.edu

  Affiliations Departments of Pediatrics and of Human Genetics, University of Michigan, Ann Arbor, Michigan, United States of America, Howard Hughes Medical Institute, University of Michigan, Ann Arbor, Michigan, United States of America

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