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Autosomal recessive cortical myoclonic tremor and epilepsy: Association with a mutation in the potassium channel associated gene CNTN2

✍ Scribed by Stögmann, E.

Book ID: 123196474
Publisher: Elsevier Science
Year: 2013
Tongue: English
Weight: 67 KB
Volume: 333
Category: Article
ISSN: 0022-510X
DOI: 10.1016/j.jns.2013.07.076

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