Display Settings:

Format

Send to:

Choose Destination
See comment in PubMed Commons below
Neurology. 1992 May;42(5):1046-8.

Evidence of genetic heterogeneity among the nondystrophic myotonias.

Author information

  • 1Department of Neurology, University of Utah School of Medicine, Salt Lake City.

Abstract

Recent in vitro electrophysiologic studies have demonstrated abnormal sodium channel gating in muscle from patients with Thomsen's disease and have called the chloride hypothesis into question. Abnormal sodium channel function, like myotonia, is a feature common to Thomsen's disease and several myotonias that are genetically linked to a chromosome-17q sodium channel locus. We present a pedigree segregating an allele for Thomsen's disease that is unlinked to this sodium channel locus, thus constituting evidence of genetic heterogeneity among the nondystrophic myotonias.

PMID:
1315941
[PubMed - indexed for MEDLINE]
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Loading ...
    Write to the Help Desk