Pseudohypoaldosteronism in a newborn male with functional polymorphisms in the mineralocorticoid receptor genes.

about

Pseudohypoaldosteronism in a newborn male with functional polymorphisms in the mineralocorticoid receptor genes.

Item

http://www.wikidata.org/entity/Q41822493

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

Pseudohypoaldosteronism in a n ...... eralocorticoid receptor genes.

@en

type

Item

label

Pseudohypoaldosteronism in a n ...... eralocorticoid receptor genes.

@en

prefLabel

Pseudohypoaldosteronism in a n ...... eralocorticoid receptor genes.

@en

P1476

Pseudohypoaldosteronism in a n ...... eralocorticoid receptor genes.

@en

P2093

Hyo-Kyoung Nam

http://www.w3.org/2001/XMLSchema#string

Hyun Ah Jeong

http://www.w3.org/2001/XMLSchema#string

Kee Hyoung Lee

http://www.w3.org/2001/XMLSchema#string

Myung-Hyun Nam

http://www.w3.org/2001/XMLSchema#string

Yeong Sang Jung

http://www.w3.org/2001/XMLSchema#string

Yoon Kyoung Park

http://www.w3.org/2001/XMLSchema#string

Young-Jun Rhie

http://www.w3.org/2001/XMLSchema#string

P2860

Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I

A salt wasting syndrome in infancy

Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1

A case of pseudohypoaldosteronism type 1 with a mutation in the mineralocorticoid receptor gene.

Pseudohypoaldosteronism type 1: clinical features and management in infancy.

The functional c.-2G>C variant of the mineralocorticoid receptor modulates blood pressure, renin, and aldosterone levels.

Functional polymorphisms in the mineralocorticoid receptor and amirolide-sensitive sodium channel genes in a patient with sporadic pseudohypoaldosteronism.

Autosomal Dominant Pseudohypoaldosteronism Type 1: Mechanisms, Evidence for Neonatal Lethality, and Phenotypic Expression in Adults

P304

230-234

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.6065/APEM.2015.20.4.230

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2015-12-31T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

291386210

http://www.w3.org/2001/XMLSchema#string

P698

26817011

http://www.w3.org/2001/XMLSchema#string

P932

4722164

http://www.w3.org/2001/XMLSchema#string