Molecular genetic finding in migraine;Molekylærgenetiske fund ved migræne

Ugeskrift for Laeger

Volumn 163, Issue 45, 2001, Pages 6260-6265

  Otergaard E ^a   Lykke Thomsen, L ^a   Bjorn Russell M ^a  

^a JOHN F KENNEDY INSTITUTE   (Denmark)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM CHANNEL; CALCIUM ION; DIPEPTIDYL CARBOXYPEPTIDASE; DOPAMINE RECEPTOR; MITOCHONDRIAL DNA; NITRIC OXIDE SYNTHASE; SEROTONIN RECEPTOR;

ATAXIA; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 19P; CHROMOSOME 1Q; CONTROLLED STUDY; GENETIC CODE; HUMAN; MIGRAINE; MOLECULAR GENETICS; MULTIFACTORIAL INHERITANCE; MUTATION; POINT MUTATION; REVIEW; SPINOCEREBELLAR DEGENERATION; X CHROMOSOME; CALCIUM CHANNEL; CEREBELLAR ATAXIA; GENETIC PREDISPOSITION; GENETICS; METABOLISM; MISSENSE MUTATION;

CALCIUM CHANNELS; CEREBELLAR ATAXIA; CLASSIC MIGRAINE; COMMON MIGRAINE; ENGLISH ABSTRACT; GENETIC PREDISPOSITION TO DISEASE; HUMAN; MIGRAINE; MUTATION, MISSENSE; POINT MUTATION; SPINOCEREBELLAR DEGENERATIONS;

EID: 0035813633     PISSN: 00415782     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

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2. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4
3. Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity
4. A new locus for hemiplegic migraine maps to chromosome 1q31
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