Ataxia and myoclonic epilepsy due to a heterozygous new mutation in KCNA2: proposal for a new channelopathy. (Q53676072)
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scientific article published in February 2015
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Ataxia and myoclonic epilepsy due to a heterozygous new mutation in KCNA2: proposal for a new channelopathy. |
scientific article published in February 2015 |
Statements
Ataxia and myoclonic epilepsy due to a heterozygous new mutation in KCNA2: proposal for a new channelopathy. (English)
S D J Pena
R L M Coimbra
1 February 2015
87
2
e1-3
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