Terwindt, G M <br/><br/>
Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group.  [electronic resource] 

 -  Neurology  Apr 1998 
 - 1105-10 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0028-3878 
<br/><br/><label>Standard No.: </label>10.1212/wnl.50.4.1105  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Brain Chemistry--genetics<br/>Calcium Channels--genetics<br/>Calcium Channels, N-Type<br/>Cerebellar Ataxia--genetics<br/>Child<br/>DNA Mutational Analysis<br/>Family Health<br/>Female<br/>Gene Expression<br/>Genotype<br/>Hemiplegia--genetics<br/>Humans<br/>Male<br/>Migraine Disorders--genetics<br/>Mutation<br/>Pedigree<br/>Phenotype<br/>Repetitive Sequences, Nucleic Acid