期刊
CURRENT OPINION IN NEUROLOGY
卷 15, 期 3, 页码 311-316出版社
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/00019052-200206000-00014
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An increasing number of mutations in the CACNA1A gene have been identified, which are associated with a broad clinical spectrum, including familial hemiplegic migraine. Transfection studies and mouse model analyses are currently being undertaken to study the correlation between CACNA1A mutations and disease.
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