Establishing the genetic heterogeneity of familial hemiplegic migraine

Brain

Volumn 130, Issue 2, 2007, Pages 312-313

  Low, Nancy ^a   Singleton, Andrew ^b  

^a NATIONAL INSTITUTE OF MENTAL HEALTH   (United States)

^b NATIONAL INSTITUTE ON AGING   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME; CLINICAL FEATURE; FAMILIAL HEMIPLEGIC MIGRAINE; GENE LOCUS; GENE MUTATION; GENETIC HETEROGENEITY; GENETIC LINKAGE; GENOTYPE PHENOTYPE CORRELATION; HUMAN; MUTATIONAL ANALYSIS; NOTE; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL;

EID: 33846563970     PISSN: 00068950     EISSN: 14602156     Source Type: Journal    
DOI: 10.1093/brain/awl381     Document Type: Note

References (9)

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3. Ducros A, Denier C, Joutel A, Vahedi K, Michel A, Darcel F, et al. Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia. Am J Hum Genet 1999; 64: 89-98.
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