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

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

Research output: Contribution to journalComment/debate

81 Scopus citations
Original languageEnglish (US)
Pages (from-to)1671-1672
Number of pages2
JournalHuman molecular genetics
Volume4
Issue number9
DOIs
StatePublished - Sep 1 1995

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Genetics(clinical)

Cite this

Browne, D. L., Brunt, E. R. P., Griggs, R. C., Nutt, J. G., 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