Prevalence of Novel MAGED2 Mutations in Antenatal Bartter Syndrome.

about

Prevalence of Novel MAGED2 Mutations in Antenatal Bartter Syndrome.

Item

http://www.wikidata.org/entity/Q47577129

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh-hant

name

Prevalence of Novel MAGED2 Mutations in Antenatal Bartter Syndrome.

@en

Prevalence of Novel MAGED2 Mutations in Antenatal Bartter Syndrome.

@nl

type

Item

label

Prevalence of Novel MAGED2 Mutations in Antenatal Bartter Syndrome.

@en

Prevalence of Novel MAGED2 Mutations in Antenatal Bartter Syndrome.

@nl

prefLabel

Prevalence of Novel MAGED2 Mutations in Antenatal Bartter Syndrome.

@en

Prevalence of Novel MAGED2 Mutations in Antenatal Bartter Syndrome.

@nl

P1476

Prevalence of Novel MAGED2 Mutations in Antenatal Bartter Syndrome.

@en

P2093

Amélie Ryckewaert

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

Anne Blanchard

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

Anne Legrand

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

Aurélia Bertholet-Thomas

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

Brigitte Llanas

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

Christine Pietrement

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

Cyrielle Treard

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

Daniele Bruno

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

Denis Morin

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

Djamal Djeddi

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

P2860

Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter

Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III

Bartter- and Gitelman-like syndromes: salt-losing tubulopathies with loop or DCT defects.

Polyhydramnios, Transient Antenatal Bartter's Syndrome, and MAGED2 Mutations

Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome

Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis. A new syndrome

Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure

Salt wasting and deafness resulting from mutations in two chloride channels

P31

scholarly article

P356

10.2215/CJN.05670517

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

P577

2017-11-16T00:00:00Z

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

P698

29146702

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

P932

5967426

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