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Ataxia and myoclonic epilepsy due to a heterozygous new mutation in KCNA2: proposal for a new channelopathy
by
Pena, S.D.J.
,
Coimbra
,
R.L.M
.
Published in
Clinical genetics
(01.02.2015)
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biology
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amino acid substitution
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animals
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ataxia
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channelopathies - genetics
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Wiley Online Library - Core collection (SURFmarket)
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