The diagnosis of Liddle syndrome by identification of a mutation in the beta subunit of the epithelial sodium channel.
about
Genetic screening of SCNN1B and SCNN1G genes in early-onset hypertensive patients helps to identify Liddle syndrome.NMD: RNA biology meets human genetic medicine.Liddle syndrome in a Serbian family and literature review of underlying mutations.Development and Diseases of the Collecting Duct System.Peptide inhibition of constitutively activated epithelial Na(+) channels expressed in Xenopus oocytes.Liddle Syndrome: Review of the Literature and Description of a New Case.
P2860
The diagnosis of Liddle syndrome by identification of a mutation in the beta subunit of the epithelial sodium channel.
description
1998 nî lūn-bûn
@nan
1998 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
The diagnosis of Liddle syndro ...... the epithelial sodium channel.
@ast
The diagnosis of Liddle syndro ...... the epithelial sodium channel.
@en
type
label
The diagnosis of Liddle syndro ...... the epithelial sodium channel.
@ast
The diagnosis of Liddle syndro ...... the epithelial sodium channel.
@en
prefLabel
The diagnosis of Liddle syndro ...... the epithelial sodium channel.
@ast
The diagnosis of Liddle syndro ...... the epithelial sodium channel.
@en
P2093
P2860
P356
P1476
The diagnosis of Liddle syndro ...... the epithelial sodium channel.
@en
P2093
Jackson SN
Trembath RC
Williams B
P2860
P304
P356
10.1136/JMG.35.6.510
P407
P577
1998-06-01T00:00:00Z