Identification of two new KCNA1 mutations in episodic ataxia/myokymia families

D. L. Browne, E. R P Brunt, R. C. Griggs, John Nutt, S. T. Gancher, E. A. Smith, M. Litt

Research output: Contribution to journalArticle

80 Citations (Scopus)
Original languageEnglish (US)
Pages (from-to)1671-1672
Number of pages2
JournalHuman Molecular Genetics
Volume4
Issue number9
DOIs
StatePublished - Sep 1995

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Molecular Sequence Data
Myokymia
Fasciculation
Potassium Channels
Ataxia
Pedigree
Point Mutation
Mutation
DNA
Episodic Ataxia

ASJC Scopus subject areas

  • Statistics, Probability and Uncertainty
  • Applied Mathematics
  • Public Health, Environmental and Occupational Health
  • Molecular Biology
  • Genetics(clinical)
  • Genetics

Cite this

Browne, D. L., Brunt, E. R. P., Griggs, R. C., Nutt, J., Gancher, S. T., Smith, E. A., & Litt, M. (1995). Identification of two new KCNA1 mutations in episodic ataxia/myokymia families. Human Molecular Genetics, 4(9), 1671-1672. https://doi.org/10.1093/hmg/4.9.1671

Identification of two new KCNA1 mutations in episodic ataxia/myokymia families. / Browne, D. L.; Brunt, E. R P; Griggs, R. C.; Nutt, John; Gancher, S. T.; Smith, E. A.; Litt, M.

In: Human Molecular Genetics, Vol. 4, No. 9, 09.1995, p. 1671-1672.

Research output: Contribution to journalArticle

Browne, DL, Brunt, ERP, Griggs, RC, Nutt, J, Gancher, ST, Smith, EA & Litt, M 1995, 'Identification of two new KCNA1 mutations in episodic ataxia/myokymia families', Human Molecular Genetics, vol. 4, no. 9, pp. 1671-1672. https://doi.org/10.1093/hmg/4.9.1671
Browne, D. L. ; Brunt, E. R P ; Griggs, R. C. ; Nutt, John ; Gancher, S. T. ; Smith, E. A. ; Litt, M. / Identification of two new KCNA1 mutations in episodic ataxia/myokymia families. In: Human Molecular Genetics. 1995 ; Vol. 4, No. 9. pp. 1671-1672.
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