Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group. [electronic resource]
Producer: 19980507Description: 1105-10 p. digitalISSN:- 0028-3878
- Adolescent
- Adult
- Brain Chemistry -- genetics
- Calcium Channels -- genetics
- Calcium Channels, N-Type
- Cerebellar Ataxia -- genetics
- Child
- DNA Mutational Analysis
- Family Health
- Female
- Gene Expression
- Genotype
- Hemiplegia -- genetics
- Humans
- Male
- Migraine Disorders -- genetics
- Mutation
- Pedigree
- Phenotype
- Repetitive Sequences, Nucleic Acid
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.