Whole-exome sequencing in an individual with severe global...

Whole-exome sequencing in an individual with severe global developmental delay and intractable epilepsy identifies a novel, de novo GRIN2A mutation

Venkateswaran, Sunita, Myers, Ken A., Smith, Amanda C., Beaulieu, Chandree L., Schwartzentruber, Jeremy A., Majewski, Jacek, Bulman, Dennis, Boycott, Kym M., Dyment, David A.
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Volume:
55
Language:
english
Journal:
Epilepsia
DOI:
10.1111/epi.12663
Date:
July, 2014
File:
PDF, 682 KB
english, 2014
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