Ataxia and myoclonic epilepsy due to a heterozygous new mutation in KCNA2: proposal for a new channelopathy

Publisher: John Wiley & Sons Inc

E-ISSN: 1399-0004|87|2|e1-e3

ISSN: 0009-9163

Source: CLINICAL GENETICS, Vol.87, Iss.2, 2015-02, pp. : e1-e3

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