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LMX1B mutations cause hereditary FSGS without extrarenal involvement.
Boyer, Olivia; Woerner, Stéphanie; Yang, Fan; Oakeley, Edward J; Linghu, Bolan; Gribouval, Olivier; Tête, Marie-Josèphe; Duca, José S; Klickstein, Lloyd; Damask, Amy J; Szustakowski, Joseph D; Heibel, Françoise; Matignon, Marie; Baudouin, Véronique; Chantrel, François; Champigneulle, Jacqueline; Martin, Laurent; Nitschké, Patrick; Gubler, Marie-Claire; Johnson, Keith J; Chibout, Salah-Dine; Antignac, Corinne.
Affiliation
  • Boyer O; Inserm U983, Hôpital Necker-Enfants Malades, Paris, France.
J Am Soc Nephrol ; 24(8): 1216-22, 2013 Jul.
Article in En | MEDLINE | ID: mdl-23687361
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Transcription Factors / Glomerulosclerosis, Focal Segmental / LIM-Homeodomain Proteins / Nail-Patella Syndrome Type of study: Prognostic_studies Limits: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Language: En Journal: J Am Soc Nephrol Journal subject: NEFROLOGIA Year: 2013 Document type: Article Affiliation country: Country of publication:
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Transcription Factors / Glomerulosclerosis, Focal Segmental / LIM-Homeodomain Proteins / Nail-Patella Syndrome Type of study: Prognostic_studies Limits: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Language: En Journal: J Am Soc Nephrol Journal subject: NEFROLOGIA Year: 2013 Document type: Article Affiliation country: Country of publication: