Molecular characterization and investigation of the role of genetic variation in phenotypic variability and response to treatment in a large pediatric Marfan syndrome cohort.

When we extended this region to exons 26 to 49, on the basis of the average aortic z-score per exon, we did observe a highly significant result, which also survived multiple hypotheses analysis ( Q = 7.6 × 10 −4 ).

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