Mutation spectrum of Chinese patients with Bartter syndrome.

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Mutation spectrum of Chinese patients with Bartter syndrome.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

@zh-sg

2017年學術文章

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2017年學術文章

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Mutation spectrum of Chinese patients with Bartter syndrome.

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Mutation spectrum of Chinese patients with Bartter syndrome.

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label

Mutation spectrum of Chinese patients with Bartter syndrome.

@en

Mutation spectrum of Chinese patients with Bartter syndrome.

@nl

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Mutation spectrum of Chinese patients with Bartter syndrome.

@en

Mutation spectrum of Chinese patients with Bartter syndrome.

@nl

P1476

Mutation spectrum of Chinese patients with Bartter syndrome.

@en

P2093

Leping Shao

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Qing Sun

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

Shujuan Wang

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

Yanxia Gao

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Yi Lin

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Yue Han

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P2860

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

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

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

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

Bartter syndrome type 3: an unusual cause of nephrolithiasis

Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome

Analysis of missense variation in human BRCA1 in the context of interspecific sequence variation

Amino acid difference formula to help explain protein evolution

Novel molecular variants of the Na-K-2Cl cotransporter gene are responsible for antenatal Bartter syndrome

Spectrum of mutations in Gitelman syndrome.

P304

101614-101622

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P31

scholarly article

P356

10.18632/ONCOTARGET.21355

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P407

English

P433

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P478

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

P577

2017-09-27T00:00:00Z

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P698

29254190

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P932

5731900

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