Pathophysiology, diagnosis and treatment of inherited distal renal tubular acidosis.

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Mouse Models of SLC4-linked Disorders of HCO3- Transporter Dysfunction.

P2860

Q49559317-44D55BDA-85E8-4309-A0B6-E669A0793C61

P2860

Pathophysiology, diagnosis and treatment of inherited distal renal tubular acidosis.

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http://www.wikidata.org/entity/Q48218609

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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

@wuu

2017年学术文章

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2017年学术文章

@zh-cn

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@zh-my

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2017年學術文章

@zh-hant

name

Pathophysiology, diagnosis and treatment of inherited distal renal tubular acidosis.

@en

Pathophysiology, diagnosis and treatment of inherited distal renal tubular acidosis.

@nl

type

Item

label

Pathophysiology, diagnosis and treatment of inherited distal renal tubular acidosis.

@en

Pathophysiology, diagnosis and treatment of inherited distal renal tubular acidosis.

@nl

prefLabel

Pathophysiology, diagnosis and treatment of inherited distal renal tubular acidosis.

@en

Pathophysiology, diagnosis and treatment of inherited distal renal tubular acidosis.

@nl

P1476

Pathophysiology, diagnosis and treatment of inherited distal renal tubular acidosis.

@en

P2093

Nilufar Mohebbi

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P2860

Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness

Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing

Non-polarized targeting of AE1 causes autosomal dominant distal renal tubular acidosis

Localization and regulation of the ATP6V0A4 (a4) vacuolar H+-ATPase subunit defective in an inherited form of distal renal tubular acidosis

Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss

Localization of a gene for autosomal recessive distal renal tubular acidosis with normal hearing (rdRTA2) to 7q33-34

Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (Band 3, AE1) gene

Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis

ClC-5, the chloride channel mutated in Dent's disease, colocalizes with the proton pump in endocytotically active kidney cells

The rhesus protein RhCG: a new perspective in ammonium transport and distal urinary acidification.

P2888

s40620-017-0447-1

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scholarly article

P356

10.1007/S40620-017-0447-1

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P50

Carsten A Wagner

P577

2017-10-09T00:00:00Z

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P698

28994037

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P921

pathophysiology

Pathophysiology, diagnosis and treatment of inherited distal renal tubular acidosis.

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P2860

P2860

Pathophysiology, diagnosis and treatment of inherited distal renal tubular acidosis.

description

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type

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prefLabel

P1433

P1476

P2093

P2860

P2888

P31

P356

P50

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P2888

P31

P356

P50

P577

P698

P921