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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

CEPHALALGIA (2008)

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CEPHALALGIA
Volume 28, Issue 4, Pages 403-407

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SAGE PUBLICATIONS LTD
DOI: 10.1111/j.1468-2982.2008.01540.x

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Clinical Neurology Neurosciences

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