Human diseases associated with connexin mutations.

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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年學術文章

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2017年學術文章

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2017年學術文章

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name

Human diseases associated with connexin mutations.

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Human diseases associated with connexin mutations.

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Item

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Human diseases associated with connexin mutations.

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Human diseases associated with connexin mutations.

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prefLabel

Human diseases associated with connexin mutations.

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Human diseases associated with connexin mutations.

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P1476

Human diseases associated with connexin mutations

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P2093

Miduturu Srinivas

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Vytas K Verselis

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P2860

Gap junction mediated intercellular metabolite transfer in the cochlea is compromised in connexin30 null mice

GJC2 missense mutations cause human lymphedema

Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis

Connexin46 mutations in autosomal dominant congenital cataract.

Somatic mutations in the connexin 40 gene (GJA5) in atrial fibrillation

Novel germline GJA5/connexin40 mutations associated with lone atrial fibrillation impair gap junctional intercellular communication

A missense mutation in the human connexin50 gene (GJA8) underlies autosomal dominant "zonular pulverulent" cataract, on chromosome 1q

Connexin mutations in X-linked Charcot-Marie-Tooth disease

Mutations in the gene encoding gap junction protein alpha 12 (connexin 46.6) cause Pelizaeus-Merzbacher-like disease

Mutation in the gene for connexin 30.3 in a family with erythrokeratodermia variabilis

P304

192-201

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scholarly article

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10.1016/J.BBAMEM.2017.04.024

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P433

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P478

1860

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P50

Thomas W. White

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2017-04-27T00:00:00Z

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P698

28457858

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5659969

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