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Could the interaction between LMX1B and PAX2 influence the severity of renal symptoms?
Negrisolo, Susanna; Carraro, Andrea; Fregonese, Giulia; Benetti, Elisa; Schaefer, Franz; Alberti, Marta; Melchionda, Salvatore; Fischetto, Rita; Giordano, Mario; Murer, Luisa.
Afiliación
  • Negrisolo S; Laboratory of Immunopathology and Molecular Biology of the Kidney, Department of Women's and Children's Health, University of Padova, Padua, Italy. susanna.negrisolo@unipd.it.
  • Carraro A; Laboratory of Immunopathology and Molecular Biology of the Kidney, Department of Women's and Children's Health, University of Padova, Padua, Italy.
  • Fregonese G; Pediatric Nephrology, Dialysis and Transplant Unit, Department of Women's and Children's Health, Hospital-University of Padova, Padua, Italy.
  • Benetti E; Pediatric Nephrology, Dialysis and Transplant Unit, Department of Women's and Children's Health, Hospital-University of Padova, Padua, Italy.
  • Schaefer F; Division of Pediatric Nephrology and KFH Children's Kidney Center, Center for Pediatrics and Adolescent Medicine, Heidelberg University Medical Center, Heidelberg, Germany.
  • Alberti M; RCCS-Istituto di Ricerche Farmacologiche "Mario Negri", Clinical Research Center for Rare Diseases "Aldo e Cele Daccò", Bergamo, Italy.
  • Melchionda S; "Centro Anna Maria Astori", Science Technology Park Kilometro Rosso, Bergamo, Italy.
  • Fischetto R; Medical Genetics Unit, IRCCS Casa Sollievo della Sofferenza Hospital, San Giovanni Rotondo, Italy.
  • Giordano M; Unit of Metabolic Disease and Medical Genetics, University Hospital, P.O. Giovanni XXIII, Bari, Italy.
  • Murer L; Unit of Pediatric Nephrology, University Hospital, P.O. Giovanni XXIII, Bari, Italy.
Eur J Hum Genet ; 26(11): 1708-1712, 2018 11.
Article en En | MEDLINE | ID: mdl-29973660
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenotipo / Factores de Transcripción / Factor de Transcripción PAX2 / Proteínas con Homeodominio LIM / Síndrome de la Uña-Rótula Tipo de estudio: Diagnostic_studies Límite: Child / Female / Humans Idioma: En Revista: Eur J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Reino Unido
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenotipo / Factores de Transcripción / Factor de Transcripción PAX2 / Proteínas con Homeodominio LIM / Síndrome de la Uña-Rótula Tipo de estudio: Diagnostic_studies Límite: Child / Female / Humans Idioma: En Revista: Eur J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Reino Unido