Familial hyperkalemic periodic paralysis : a brief review of the adult human skeletal muscle sodium channel and the application of LA-PCR to the SCN4A gene analysis

Recent work has revealed that familial hyperkalemic periodic paralysis, paramyotonia congenita and other non-dystrophic myotonias result from point mutations in the gene encoding the alpha-subunit of the adult human skeletal muscle sodium channel (SCN4A). Sodium channel myotonias are a diverse group...

Full description

Bibliographic Details
Published in:Nihon rinsho. Japanese journal of clinical medicine, Vol. 55, No. 12 (1997), p. 3253-8
Main Author: Sakoda, S
Other Involved Persons: Nakagawa, M ; Arimura, Y ; Arimura, K ; Osame, M
Format: Article
Language:Japanese
ISSN:0047-1852
Item Description:Date Completed 24.03.1998
Date Revised 27.07.2011
published: Print
Citation Status MEDLINE
Copyright: From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
Subjects:
QR Code: Show QR Code