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Exome sequencing reveals new causal mutations in children with epileptic encephalopathies

✍ Scribed by Veeramah, Krishna R.; Johnstone, Laurel; Karafet, Tatiana M.; Wolf, Daniel; Sprissler, Ryan; Salogiannis, John; Barth-Maron, Asa; Greenberg, Michael E.; Stuhlmann, Till; Weinert, Stefanie; Jentsch, Thomas J.; Pazzi, Marjorie; Restifo, Linda L.; Talwar, Dinesh; Erickson, Robert P.; Hammer, Michael F.

Book ID: 120932662
Publisher: Wiley (Blackwell Publishing)
Year: 2013
Tongue: English
Weight: 414 KB
Volume: 54
Category: Article
ISSN: 0013-9580
DOI: 10.1111/epi.12201

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