California Birth Defects Monitoring Program, Berkeley
NPPA appears to be a good candidate gene for conotruncal defects
Published in Cardiovascular Device Liability Week, November 6th, 2005
According to investigators in the United States, "Investigating possible genetic polymorphisms and gene-environment interactions in the etiology of human conotruncal defects is a prudent research approach. In [our] study we explore gene-only and gene-environment effects of 32 single nucleotide polymorphisms (SNPs) on conotruncal defect risks."
G.M. Shaw and colleagues of the California Birth Defects Monitoring Program explained, "The genes bearing these SNPs participate in one...
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