Work

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

Year: 1994

Type: article

Study design: Observational Study

Source: Nature Genetics

DOI: 10.1038/ng1094-136

Authors: David L. Browne, Stephen T. Gancher, John G. Nutt, Ewout R. P. Brunt, Eric A. Smith, Patricia Kramer, Michael Litt

Institutions: Oregon Health & Science University, University Medical Center Groningen

Language: English

Topic: Ion channel regulation and function

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: National Human Genome Research Institute, National Institute of Neurological Disorders and Stroke

Awards: G1214034672, NEUROLOGICAL DISEASE GENE MAPPING DNA EPIOSODIC

OpenAlex ID: W2142980147

FWCI: 6.582

Cites: 20

Cited by: 776

Related to: 10