De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies



Myers, Candace T, McMahon, Jacinta M, Schneider, Amy L, Petrovski, Slave, Allen, Andrew S, Carvill, Gemma L, Zemel, Matthew, Say-Kally, Julia E, LaCroix, Amy J, Heinzen, Erin L
et al (show 35 more authors) (2016) De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies. AMERICAN JOURNAL OF HUMAN GENETICS, 99 (2). 287 - 298.

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Item Type: Article
Depositing User: Symplectic Admin
Date Deposited: 03 Jan 2018 11:41
Last Modified: 29 Jul 2021 14:12
DOI: 10.1016/j.ajhg.2016.06.003
Open Access URL: http://www.cell.com/ajhg/fulltext/S0002-9297(16)30...
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URI: https://livrepository.liverpool.ac.uk/id/eprint/3015345