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.
Item Type: | Article |
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Depositing User: | Symplectic Admin |
Date Deposited: | 03 Jan 2018 11:41 |
Last Modified: | 19 May 2022 15:09 |
DOI: | 10.1016/j.ajhg.2016.06.003 |
Open Access URL: | http://www.cell.com/ajhg/fulltext/S0002-9297(16)30... |
Related URLs: | |
URI: | https://livrepository.liverpool.ac.uk/id/eprint/3015345 |
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