(Q28137646)

English

Deafness and imbalance associated with inactivation of the secretory Na-K-2Cl co-transporter

scientific article (publication date: June 1999)

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scholarly article

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Deafness and imbalance associated with inactivation of the secretory Na-K-2Cl co-transporter (English)

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author name string

E Delpire

1

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J Lu

2

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R England

3

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C Dull

4

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T Thorne

5

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publication date

June 1999

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Nature Genetics

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22

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192-5

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2

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Genes responsible for human hereditary deafness: symphony of a thousand

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KCNE1 mutations cause jervell and Lange-Nielsen syndrome

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A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

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Inner ear defects induced by null mutation of the isk gene

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KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness

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The Na-K-Cl cotransporters.

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

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Primary structure, functional expression, and chromosomal localization of the bumetanide-sensitive Na-K-Cl cotransporter in human colon

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Molecular and clinical implications of loop diuretic ototoxicity

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The fundamental and medical impacts of recent progress in research on hereditary hearing loss.

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Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous

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