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In fact, several recent studies that have conducted genome wide searches for common genetic defects across large samples of ASD children have only identified rare de novo mutations, thereby pointing to acquired mutations and/or mutations secondary to errors in DNA maintenance rather than inherited genetic syndromes (11, 12)
DXA versus clinical measures of adiposity as predictors of cardiometabolic diseases and all-cause mortality in postmenopausal women
Treatment for hyperammonemic encephalopathy from valproic acid includes valproic acid cessation +/- levocarnitine treatment
