Different gene loci for hyperkalemic and hypokalemic periodic paralysis

scientific article published on 01 January 1991

Different gene loci for hyperkalemic and hypokalemic periodic paralysis is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/0960-8966(91)90095-A
P953full work available at URLhttps://api.elsevier.com/content/article/PII:096089669190095A?httpAccept=text/plain
https://api.elsevier.com/content/article/PII:096089669190095A?httpAccept=text/xml
P698PubMed publication ID1822800

P50authorJames F. GusellaQ1602688
Guy A. RouleauQ3121500
Jonathan L HainesQ73570557
P2093author name stringR. Brown
B. Fontaine
J. Haines
T. S. Khurana
J. Trofatter
P2860cites workA technique for radiolabeling DNA restriction endonuclease fragments to high specific activityQ26778490
Strategies for multilocus linkage analysis in humansQ27860521
Hyperkalemic periodic paralysis and the adult muscle sodium channel alpha-subunit geneQ28242463
Hypokalemic periodic paralysis: In vitro investigation of muscle fiber membrane parametersQ28265960
Paramyotonia congenita or hyperkalemic periodic paralysis? Clinical and electrophysiological features of each entity in one familyQ28281836
A polymorphic DNA marker genetically linked to Huntington's diseaseQ34255139
Patterns of polymorphism and linkage disequilibrium suggest independent origins of the human growth hormone gene clusterQ37570769
Probing the molecular structure of the voltage-dependent sodium channelQ38187876
Structure and function of voltage-sensitive ion channelsQ38193558
Primary structure and expression of a sodium channel characteristic of denervated and immature rat skeletal muscleQ41745813
Primary structure and functional expression of a mammalian skeletal muscle sodium channelQ42189395
A computer program for linkage analysis of general human pedigreesQ43144003
Abnormalities of the fast sodium current in myotonic dystrophy, recessive generalized myotonia, and adynamia episodicaQ44071015
Schwartz-Jampel syndrome: II. Na+ channel defect causes myotoniaQ44358032
A sodium channel defect in hyperkalemic periodic paralysis: potassium-induced failure of inactivationQ67915164
Adynamia episodica hereditaria with myotonia: a non-inactivating sodium current and the effect of extracellular pHQ69033394
Membrane defects in paramyotonia congenita (Eulenburg)Q69406285
P433issue4
P407language of work or nameEnglishQ1860
P921main subjectneurologyQ83042
hypokalemic periodic paralysisQ622828
P304page(s)235-238
P577publication date1991-01-01
P1433published inNeuromuscular DisordersQ1981326
P1476titleDifferent gene loci for hyperkalemic and hypokalemic periodic paralysis
P478volume1