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Published in 2020 at "Human Cell"
DOI: 10.1007/s13577-020-00374-2
Abstract: Trisomy 21 or Down syndrome (DS) is the most frequent genetic etiology of intellectual disability in humans. MDM2 gene expression has a potential role as a risk factor for human aneuploidy. -410T-G (rs2279744) functional polymorphism…
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Keywords:
study mdm2;
410t polymorphism;
mdm2 410t;
rs2279744 pyrosequencing ... See more keywords