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Pediatric Neurology
Volume 26, Issue 1
, Pages
47-50
, January 2002
Wide clinical variability in a family with a CACNA1A T666m mutation: hemiplegic migraine, coma, and progressive ataxia
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PII: S0887-8994(01)00371-X
© 2002 Elsevier Science Inc. All rights reserved.
« Previous
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Pediatric Neurology
Volume 26, Issue 1
, Pages
47-50
, January 2002
