A novel homozygous mutation in the solute carrier family 12 member 3 gene in a Chinese family with Gitelman syndrome
2016 ◽
Vol 49
(11)
◽
Keyword(s):
2021 ◽
pp. bjophthalmol-2020-318204
2019 ◽
Vol 20
(10)
◽
pp. 2493
◽
2013 ◽
Vol 34
(2-3)
◽
pp. 252-269
◽
Keyword(s):
2007 ◽
Vol 49
(3)
◽
pp. 324-329
◽
2006 ◽
Vol 208
(1)
◽
pp. 25-31
◽
2013 ◽
Vol 2
(6)
◽
pp. 227-239
◽