Heterocigosis compuesta para las mutaciones Intron 9 + 1 g > T y Leu850pro en el gen SLC12A3 en el Síndrome de Gitelman
Compound heterozygosis for intrón 9 + 1 g > T and Leu 850pro mutations in the SLC12A3 gene in Gitelman¿s syndrome
a Servicio de Nefrología, Fundación Jiménez Díaz-Capio, Madrid, Madrid, España,
b 3Hospital La Paz. Universidad Autónoma de Madrid, Madrid, Madrid, España,
c Servicio de Nefrología, Fundación Jiménez Díaz-Capio, Madrid, MadridMadrid, España,
d 1Unidad de Genética Molecular Hospital Central de Asturias e Instituto de Estudios Nefrológicos. Asturias Asturias España,
e Unidad de Nefrología pediátrica, Hospital Central de Asturias e Instituto de Estudios Nefrológicos. Asturias Asturias España,
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