reference/19409625

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/19409625

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endingPage	354
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bibliographicCitation	Ohmori I, Ouchida M, Miki T, Mimaki N, Kiyonaka S, Nishiki T, Tomizawa K, Mori Y, Matsui H. A CACNB4 mutation shows that altered Ca(v)2.1 function may be a genetic modifier of severe myoclonic epilepsy in infancy. Neurobiol Dis. 2008 Dec;32(3):349–54. doi: 10.1016/j.nbd.2008.07.017. PMID: 18755274.
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date	200812
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language	English
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title	A CACNB4 mutation shows that altered Ca(v)2.1 function may be a genetic modifier of severe myoclonic epilepsy in infancy
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