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

Publisher： John Wiley & Sons Inc

E-ISSN： 1528-1167|55|7|e75-e79

ISSN： 0013-9580

Source： EPILEPSIA, Vol.55, Iss.7, 2014-07, pp. : e75-e79

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