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Duplication of MAOA, MAOB, and NDP in a patient with mental retardation and epilepsy.
Eur J Hum Genet 19(1):1-2 (2011) PMID 20808325
DOI: 10.1038/ejhg.2010.149
Version: za2963e q8za3 q8zbc q8zc7 q8zd6 q8ze3 q8zfc q8zg4
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Eur J Hum Genet 19(1):1-2 (2011) PMID 20808325
DOI: 10.1038/ejhg.2010.149
Am J Hum Genet 86(5):16 (2010) PMID 20466091
Am J Hum Genet 87(2):10 (2010) PMID 20673865
Pathogenetics 3(1):2 (2010) PMID 20181063