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Loss of function of mutated solute carrier family 12 member 3 (SLC12A3) gene is the most frequent et...
BACKGROUND: Loss-of-function mutations in SLC12A3 coding for the thiazide-sensitive NaCl cotransport...
Gitelman's syndrome (GS) is a relatively frequent salt-losing tubulopathy caused by mutations in the...
Abstract Background Gitelman syndrome (GS) is an autosomal recessive disorder caused by genic mutati...
Gitelman syndrome (GS) is a recessive salt-losing tubulopathy that is caused by mutations in the SLC...
Gitelman's syndrome (GS) is a salt-losing tubulopathy characterized by hypokalemic alkalosis with hy...
Abstract Background Gitelman syndrome (GS) is an autosomal recessive disorder and mild variant of cl...
Gitelman's syndrome (GS) is a salt-losing tubulopathy with an autosomal recessive inheritance caused...
Gitelman syndrome (GS) is a recessive salt-losing tubulopathy that is caused by mutations in the SLC...
Item does not contain fulltextBACKGROUND: Loss-of-function mutations in SLC12A3 coding for the thiaz...
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAM...
Abstract Recurrent mutations in the SLC12A3 gene responsible for autosomal recessive Gitelman syndro...
Gitelman's syndrome (GS) is a rare, autosomal recessive, salt-losing tubulopathy caused by mutations...
International audienceGitelman's syndrome (GS) is a rare, autosomal recessive, salt-losing tubulopat...
Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome...
Loss of function of mutated solute carrier family 12 member 3 (SLC12A3) gene is the most frequent et...
BACKGROUND: Loss-of-function mutations in SLC12A3 coding for the thiazide-sensitive NaCl cotransport...
Gitelman's syndrome (GS) is a relatively frequent salt-losing tubulopathy caused by mutations in the...
Abstract Background Gitelman syndrome (GS) is an autosomal recessive disorder caused by genic mutati...
Gitelman syndrome (GS) is a recessive salt-losing tubulopathy that is caused by mutations in the SLC...
Gitelman's syndrome (GS) is a salt-losing tubulopathy characterized by hypokalemic alkalosis with hy...
Abstract Background Gitelman syndrome (GS) is an autosomal recessive disorder and mild variant of cl...
Gitelman's syndrome (GS) is a salt-losing tubulopathy with an autosomal recessive inheritance caused...
Gitelman syndrome (GS) is a recessive salt-losing tubulopathy that is caused by mutations in the SLC...
Item does not contain fulltextBACKGROUND: Loss-of-function mutations in SLC12A3 coding for the thiaz...
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAM...
Abstract Recurrent mutations in the SLC12A3 gene responsible for autosomal recessive Gitelman syndro...
Gitelman's syndrome (GS) is a rare, autosomal recessive, salt-losing tubulopathy caused by mutations...
International audienceGitelman's syndrome (GS) is a rare, autosomal recessive, salt-losing tubulopat...
Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome...
Loss of function of mutated solute carrier family 12 member 3 (SLC12A3) gene is the most frequent et...
BACKGROUND: Loss-of-function mutations in SLC12A3 coding for the thiazide-sensitive NaCl cotransport...
Gitelman's syndrome (GS) is a relatively frequent salt-losing tubulopathy caused by mutations in the...
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