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Article

Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation.

Cephalalgia : an international journal of headache - 1 Apr 2008

Freilinger T, Bohe M, Wegener B, Müller-Myhsok B, Dichgans M, Knoblauch H

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 18279427
DOI: 10.1111/j.1468-2982.2008.01540.x

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Related research

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Research trail→

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Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation.PMID 18279427Read ↗

Phenotypic variability in a four generation family with a p.Thr666Met CACNA1A gene mutation.Semantic proximity Read ↗

CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy.Semantic proximity Read ↗

Japanese cases of familial hemiplegic migraine with cerebellar ataxia carrying a T666M mutation in the CACNA1A gene.Semantic proximity Read ↗

Wide clinical variability in a family with a CACNA1A T666m mutation: hemiplegic migraine, coma, and progressive ataxia.Semantic proximity Read ↗

CACNA1A Gene Variants in Eight Chinese Patients With a Wide Range of PhenotypesSemantic proximity Read ↗

Cerebellar ataxia, hemiplegic migraine, and related phenotypes due to a CACNA1A missense mutation: 12-year follow-up of a large Portuguese family.Semantic proximity Read ↗

Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraine.Semantic proximity Read ↗

Expanding the Phenotypic Spectrum of CACNA1H MutationsSemantic proximity Read ↗

CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine.Semantic proximity Read ↗

CACNA1A-Related Channelopathies: Clinical Manifestations and Treatment Options.Semantic proximity Read ↗

Rare CACNA1A mutations leading to congenital ataxia.Semantic proximity Read ↗

From Genotype to Phenotype: Expanding the Clinical Spectrum of CACNA1A Variants in the Era of Next Generation SequencingSemantic proximity Read ↗

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