Gene symbol: SCNN1B. Disease: Pseudohypoaldosteronism, type 1

Abstract

Peer reviewed

C P Thomas, Jackie Zhou, Kang Z Liu, Verity E Mick, Eithne MacLaughlin and Michael Knowles

Human genetics, Vol.114(4), pp.402-402

03/2004

PMID: 15046051

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Phenotype

Epithelial Sodium Channels

Homozygote

Humans

Male

Pseudohypoaldosteronism - classification

Pseudohypoaldosteronism - genetics

Sequence Deletion

Sodium Channels - genetics

Title: Subtitle: Gene symbol: SCNN1B. Disease: Pseudohypoaldosteronism, type 1
Creators: C P Thomas - Department of Internal Medicine, University of Iowa, Iowa City 52242, USA. christie-thomas@uiowa.edu
Jackie Zhou
Kang Z Liu
Verity E Mick
Eithne MacLaughlin
Michael Knowles
Resource Type: Abstract
Publication Details: Human genetics, Vol.114(4), pp.402-402
PMID: 15046051
ISSN: 0340-6717
eISSN: 1432-1203
Comment: DOI: 10.1007/s00439-004-1090-1
Language: English
Date published: 03/2004
Academic Unit: Stead Family Department of Pediatrics; Obstetrics and Gynecology; Nephrology; Internal Medicine
Record Identifier: 9984359858502771

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