Identification of two novel mutations in SLC12A3 gene in two Chinese pedigrees with Gitelman syndrome and review of literature.
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 SLC12A3 gene homozygous mutation of Gitelman syndrome in an Asian pedigree and literature review.A Pedigree with c.179 Cytosine to Threonine Missense Mutation of SLC12A3 Gene Presenting Gitelman's Syndrome.A novel compound heterozygous variant of the SLC12A3 gene in Gitelman syndrome pedigree.Identification of a novel compound heterozygous mutation of the CYP21A2 gene causing 21‑hydroxylase deficiency in a Chinese pedigree.
P2860
Identification of two novel mutations in SLC12A3 gene in two Chinese pedigrees with Gitelman syndrome and review of literature.
description
2015 nî lūn-bûn
@nan
2015 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի մայիսին հրատարակված գիտական հոդված
@hy
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
name
Identification of two novel mu ...... rome and review of literature.
@ast
Identification of two novel mu ...... rome and review of literature.
@en
type
label
Identification of two novel mu ...... rome and review of literature.
@ast
Identification of two novel mu ...... rome and review of literature.
@en
prefLabel
Identification of two novel mu ...... rome and review of literature.
@ast
Identification of two novel mu ...... rome and review of literature.
@en
P2093
P2860
P356
P1476
Identification of two novel mu ...... rome and review of literature.
@en
P2093
Congcong Li
Qingbo Guan
Wenxia Han
Xinli Zhou
P2860
P304
P356
10.1111/CEN.12820
P50
P577
2015-05-18T00:00:00Z