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Gitelman syndrome in Gypsy paediatric patients carrying the same intron 9 + 1 G>T mutation. Clinical features and impact on quality of life

Author:
Herrero Morín, José DavidUniovi authority; Rodríguez Suárez, JuliánUniovi authority; Coto García, EliecerUniovi authority; Gil Peña, HelenaUniovi authority; Álvarez Martínez, María VictoriaUniovi authority; Espinosa Román, Laura; Loris Pablo, César; Gil Calvo, Marta; Santos Rodríguez, FernandoUniovi authority
Publication date:
2011
Publisher version:
http://dx.doi.org/10.1093/ndt/gfq352
Citación:
Nephrology Dialysis Transplantation, 26(1), p. 151-155 (2011); doi:10.1093/ndt/gfq352
Descripción física:
p. 151-155
URI:
http://hdl.handle.net/10651/10126
ISSN:
0931-0509
Identificador local:

20110045

DOI:
10.1093/ndt/gfq352
Patrocinado por:

Part of this work was presented at the 4th Joint Meeting of the Spanish and Portuguese Societies of Paediatric Nephrology (Tarragona, Spain, 2005) and at the 32nd Annual Meeting of the Spanish Society of Pediatric Nephrology (Oviedo, Spain, 2006).

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