Boerman, R H <br/><br/>
Mutation in DHP receptor alpha 1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis.  [electronic resource] 

 -  Journal of medical genetics  Jan 1995 
 - 44-7 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0022-2593 
<br/><br/><label>Standard No.: </label>10.1136/jmg.32.1.44  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Age of Onset<br/>Arginine--genetics<br/>Base Sequence<br/>Calcium Channels--genetics<br/>Calcium Channels, L-Type<br/>Child<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 1<br/>DNA Primers<br/>Female<br/>Genes, Dominant<br/>Genetic Linkage<br/>Histidine--genetics<br/>Humans<br/>Hypokalemia--genetics<br/>Male<br/>Molecular Sequence Data<br/>Muscle Proteins--genetics<br/>Netherlands<br/>Paralyses, Familial Periodic--blood<br/>Pedigree<br/>Point Mutation<br/>Receptors, Cholinergic--genetics