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Nephrotic Syndrome With Mutations in NPHS2: The Role of R229Q and Implications for Genetic Counseling.
Rood, Ilse M; Deegens, Jeroen K J; Lugtenberg, Dorien; Bongers, Ernie M H F; Wetzels, Jack F M.
Affiliation
  • Rood IM; Department of Nephrology, Radboud University Medical Center, Radboud Institute for Health Sciences, Nijmegen, the Netherlands. Electronic address: ilse.rood@radboudumc.nl.
  • Deegens JKJ; Department of Nephrology, Radboud University Medical Center, Radboud Institute for Health Sciences, Nijmegen, the Netherlands.
  • Lugtenberg D; Department of Human Genetics, Radboud University Medical Center, Radboud Institute for Health Sciences, Nijmegen, the Netherlands.
  • Bongers EMHF; Department of Human Genetics, Radboud University Medical Center, Radboud Institute for Health Sciences, Nijmegen, the Netherlands.
  • Wetzels JFM; Department of Nephrology, Radboud University Medical Center, Radboud Institute for Health Sciences, Nijmegen, the Netherlands.
Am J Kidney Dis ; 73(3): 400-403, 2019 03.
Article in En | MEDLINE | ID: mdl-30241959
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Intracellular Signaling Peptides and Proteins / Genetic Counseling / Membrane Proteins / Mutation / Nephrotic Syndrome Limits: Humans Language: En Journal: Am J Kidney Dis Year: 2019 Document type: Article Country of publication:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Intracellular Signaling Peptides and Proteins / Genetic Counseling / Membrane Proteins / Mutation / Nephrotic Syndrome Limits: Humans Language: En Journal: Am J Kidney Dis Year: 2019 Document type: Article Country of publication: