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The 5-phosphatase OCRL in Lowe syndrome and Dent disease 2.
De Matteis, Maria Antonietta; Staiano, Leopoldo; Emma, Francesco; Devuyst, Olivier.
Affiliation
  • De Matteis MA; Telethon Institute of Genetics and Medicine, Via Campi Flegrei 34, 80078, Pozzuoli, Italy.
  • Staiano L; University of Naples Federico II, Via S. Pansini 5, 80131, Naples, Italy.
  • Emma F; Telethon Institute of Genetics and Medicine, Via Campi Flegrei 34, 80078, Pozzuoli, Italy.
  • Devuyst O; Division of Nephrology and Dialysis, Bambino Gesù Children's Hospital, Piazza S. Onofrio 4 00165, Rome, Italy.
Nat Rev Nephrol ; 13(8): 455-470, 2017 Aug.
Article in En | MEDLINE | ID: mdl-28669993
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phosphoric Monoester Hydrolases / Genetic Diseases, X-Linked / Nephrolithiasis / Mutation / Oculocerebrorenal Syndrome Limits: Animals / Humans Language: En Journal: Nat Rev Nephrol Journal subject: NEFROLOGIA Year: 2017 Document type: Article Affiliation country: Italia Country of publication: Reino Unido
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phosphoric Monoester Hydrolases / Genetic Diseases, X-Linked / Nephrolithiasis / Mutation / Oculocerebrorenal Syndrome Limits: Animals / Humans Language: En Journal: Nat Rev Nephrol Journal subject: NEFROLOGIA Year: 2017 Document type: Article Affiliation country: Italia Country of publication: Reino Unido