(Q28314940)

GOA release 2020-03-11

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Brett Spear

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Daniel L. Burgess

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David C. Kohrman

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James Galt

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Nicholas W. Plummer

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Julie M. Jones

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Miriam H. Meisler

Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1

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language of work or name

English

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publication date

August 1995

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1 reference

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461-465

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cites work

1 reference

https://api.crossref.org/works/10.1038/NG0895-461

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0895-461

Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPase

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0895-461

Basic local alignment search tool

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0895-461

Hereditary motor end-plate disease in the mouse: light and electron microscopic studies

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0895-461

7 January 2021

A cerebellar abnormality in the mouse with motor end-plate disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0895-461

7 January 2021

Hereditary motor endplate disease (med) of the mouse: observations on dissociated myogenic cells and their development in culture.

1 reference

https://api.crossref.org/works/10.1038%2FNG0895-461

7 January 2021

Insertional mutation of the motor endplate disease (med) locus on mouse chromosome 15.

1 reference

https://api.crossref.org/works/10.1038%2FNG0895-461

7 January 2021

Cellular and molecular biology of voltage-gated sodium channels

1 reference

https://api.crossref.org/works/10.1038%2FNG0895-461

7 January 2021

Structure, function and expression of voltage-dependent sodium channels

1 reference

https://api.crossref.org/works/10.1038%2FNG0895-461

7 January 2021

Analysis of the dopamine receptor family in the compact genome of the puffer fish Fugu rubripes

1 reference

https://api.crossref.org/works/10.1038%2FNG0895-461

7 January 2021

Calcium channel characteristics conferred on the sodium channel by single mutations

1 reference

https://api.crossref.org/works/10.1038%2FNG0895-461

7 January 2021

Genetic mapping of the spinocerebellar ataxia 2 (SCA2) locus on chromosome 12q23–q24.1

1 reference

https://api.crossref.org/works/10.1038%2FNG0895-461

7 January 2021

A mouse genomic library in the bacteriophage P1 cloning system: organization and characterization

1 reference

https://api.crossref.org/works/10.1038%2FNG0895-461

7 January 2021

Magnetic bead capture of expressed sequences encoded within large genomic segments

1 reference

https://api.crossref.org/works/10.1038%2FNG0895-461

7 January 2021

A transcription map of the region containing the Huntington disease gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0895-461

7 January 2021

Isolation of genes from complex sources of mammalian genomic DNA using exon amplification

1 reference

https://api.crossref.org/works/10.1038%2FNG0895-461

7 January 2021

A salivary amylase transgene is efficiently expressed in liver but not in parotid gland of transgenic mice

1 reference

https://api.crossref.org/works/10.1038%2FNG0895-461

7 January 2021

Preparation and screening of an arrayed human genomic library generated with the P1 cloning system

1 reference

https://api.crossref.org/works/10.1038%2FNG0895-461

7 January 2021

Mapping of the gene for interferon‐inducible dsRNA‐dependent protein kinase to chromosome region 2p21‐22: A site of rearrangements in myeloproliferative disorders

1 reference

https://api.crossref.org/works/10.1038%2FNG0895-461

7 January 2021