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. 2013 Jul 2;1(4):206–222. doi: 10.1002/mgg3.24

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© 2013 The Author. Molecular Genetics & Genomic Medicine published by Wiley Periodicals, Inc.

Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.

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Pedigrees of patients with the identified gene variants. (A) Mutations in the CACNA1A gene. (B) Mutations in the ATP1A2 gene. Affected individuals are denoted by solid symbols; hemiplegic migraine (HM) in black and other phenotypes in gray; squares indicate males and circles females. Probands are indicated by a black arrow. Clinical characteristics are indicated below each individual (HM, migraine with hemiplegic aura; MA, migraine with aura; CA, cerebellar atrophy; EA2, episodic ataxia type 2). Gene variant carrier status is indicated below each patient when known. Mutation p.Ser218Leu appeared de novo in the affected sib.