scholarly article | Q13442814 |
P356 | DOI | 10.1016/0960-8966(91)90095-A |
P953 | full work available at URL | https://api.elsevier.com/content/article/PII:096089669190095A?httpAccept=text/plain |
https://api.elsevier.com/content/article/PII:096089669190095A?httpAccept=text/xml | ||
P698 | PubMed publication ID | 1822800 |
P50 | author | James F. Gusella | Q1602688 |
Guy A. Rouleau | Q3121500 | ||
Jonathan L Haines | Q73570557 | ||
P2093 | author name string | R. Brown | |
B. Fontaine | |||
J. Haines | |||
T. S. Khurana | |||
J. Trofatter | |||
P2860 | cites work | A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity | Q26778490 |
Strategies for multilocus linkage analysis in humans | Q27860521 | ||
Hyperkalemic periodic paralysis and the adult muscle sodium channel alpha-subunit gene | Q28242463 | ||
Hypokalemic periodic paralysis: In vitro investigation of muscle fiber membrane parameters | Q28265960 | ||
Paramyotonia congenita or hyperkalemic periodic paralysis? Clinical and electrophysiological features of each entity in one family | Q28281836 | ||
A polymorphic DNA marker genetically linked to Huntington's disease | Q34255139 | ||
Patterns of polymorphism and linkage disequilibrium suggest independent origins of the human growth hormone gene cluster | Q37570769 | ||
Probing the molecular structure of the voltage-dependent sodium channel | Q38187876 | ||
Structure and function of voltage-sensitive ion channels | Q38193558 | ||
Primary structure and expression of a sodium channel characteristic of denervated and immature rat skeletal muscle | Q41745813 | ||
Primary structure and functional expression of a mammalian skeletal muscle sodium channel | Q42189395 | ||
A computer program for linkage analysis of general human pedigrees | Q43144003 | ||
Abnormalities of the fast sodium current in myotonic dystrophy, recessive generalized myotonia, and adynamia episodica | Q44071015 | ||
Schwartz-Jampel syndrome: II. Na+ channel defect causes myotonia | Q44358032 | ||
A sodium channel defect in hyperkalemic periodic paralysis: potassium-induced failure of inactivation | Q67915164 | ||
Adynamia episodica hereditaria with myotonia: a non-inactivating sodium current and the effect of extracellular pH | Q69033394 | ||
Membrane defects in paramyotonia congenita (Eulenburg) | Q69406285 | ||
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | neurology | Q83042 |
hypokalemic periodic paralysis | Q622828 | ||
P304 | page(s) | 235-238 | |
P577 | publication date | 1991-01-01 | |
P1433 | published in | Neuromuscular Disorders | Q1981326 |
P1476 | title | Different gene loci for hyperkalemic and hypokalemic periodic paralysis | |
P478 | volume | 1 |