Rune R. Frants
- Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4
1996/11/01 by Roel A. Ophoff, Roel A Ophoff, Gisela M. Terwindt +25 · 1,847 citations
Biochemistry, Genetics and Molecular Biology · Medicine · Neuroscience · Psychology · #Ataxia #Aura #Biology #Familial hemiplegic migraine #Gene #Genetic Neurodegenerative Diseases #Genetics #Migraine #Migraine with aura #Mitochondrial Function and Pathology #Mutation #Neurological disorders and treatments #Neuroscience #Psychiatry #Psychology
- Episodic Ataxia Type 2 (EA2) and Spinocerebellar Ataxia Type 6 (SCA6) Due to CAG Repeat Expansion in the CACNA1A Gene on Chromosome 19p
1997/10/01 by Carla Jodice, Elide Mantuano, Liana Veneziano +10 · 294 citations
Neuroscience · Medicine · #Genetic Neurodegenerative Diseases #Neurological disorders and treatments #Parkinson's Disease Mechanisms and Treatments #Biology #Genetics #Allele #Spinocerebellar ataxia #Ataxia #Familial hemiplegic migraine #Exon #Trinucleotide repeat expansion #Point mutation #Cerebellar ataxia #Mutation #Gene #Migraine with aura #Internal medicine #Neuroscience #Medicine