Whole-exome sequencing in an individual with severe global developmental delay and intractable epilepsy identifies a novel, de novo GRIN2A mutation.
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| Description | scientific article |
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author: Jeremy Schwartzentruber Jacek Majewski FORGE Canada Chandree L Beaulieu Kenneth Myers Dennis E Bulman Kym M Boycott |
| Publication date | June 5, 2014 |
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| Missing/wrong data? | Edit Wikidata item |