A novel SLC12A3 gene homozygous mutation of Gitelman syndrome in an Asian pedigree and literature review.
about
Hypokalemia, hypomagnesemia, hypocalciuria, and recurrent tetany: Gitelman syndrome in a Chinese pedigree and literature review.A novel homozygous mutation in the solute carrier family 12 member 3 gene in a Chinese family with Gitelman syndrome.A novel compound heterozygous variant of the SLC12A3 gene in Gitelman syndrome pedigree.
P2860
A novel SLC12A3 gene homozygous mutation of Gitelman syndrome in an Asian pedigree and literature review.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
A novel SLC12A3 gene homozygou ...... edigree and literature review.
@en
type
label
A novel SLC12A3 gene homozygou ...... edigree and literature review.
@en
prefLabel
A novel SLC12A3 gene homozygou ...... edigree and literature review.
@en
P2093
P2860
P1476
A novel SLC12A3 gene homozygou ...... edigree and literature review.
@en
P2093
P2860
P2888
P304
P356
10.1007/S40618-015-0371-Y
P577
2015-08-11T00:00:00Z
P6179
1008751344