The length of FOXE1 polyalanine tract in congenital hypothyroidism: Evidence for a pathogenic role from familial, molecular and cohort studies.

In both groups the most frequent alleles were Ala-14 and Ala-16 ( Supplementary Table 2 ), but the Ala-14/14 homozygous genotype was predominant in CH patients, either in absolute numbers and in percentages ( Supplementary Table 2 , Figure 3A ), with a highly significant X 2 test for trends (p<0.0001).

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