Mutation of a new sodium channel gene, Scn8a, in the mouse mutant ‘motor endplate disease’ (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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A cerebellar abnormality in the mouse with motor end-plate disease

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

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Calcium channel characteristics conferred on the sodium channel by single mutations

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