| http://www.w3.org/ns/prov#value | - defects such as corpus callosum agen-esis, Hirschsprung disease, and variable congenital malforma-tions such as heart and craniofacial defects (Dastot-Le Moalet al., 2007; Garavelli and Mainardi, 2007; Zweier et al., 2005).This single-gene disorder also leads to delayed motor develop-ment, seizures, and epilepsy in many MWS patients.
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