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The Utility of Exome Sequencing for Genetic Diagnosis in a Familial Microcephaly Epilepsy Syndrome.

Laura M McDonell,Jodi Warman Chardon,Jeremy Schwartzentruber, Denise Foster,Chandree L Beaulieu, FORGE Canada Consortium,Jacek Majewski,Dennis E Bulman,Kym M Boycott

BMC Neurology（2014）

Cited 24|Views7
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Key words
Primary microcephaly,Epilepsy,Whole-exome sequencing,WDR62
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