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"Common polymorphisms in ITGA2, PON1 and THBS2 are associated with coronary atherosclerosis in a candidate gene association study of the Chinese Han population"
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Studien deuten darauf hin, dass die krpereigene Glutathion-Produktion ab dem 40
ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency
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Also, they state the odds of assembling just a single gene by random mutations is between 4.3X10 -109 and 1.8X10 -217
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