Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-Situ.

J Clin Endocrinol Metab · 2016 · PMC5155683 · PMID 27525530

Europe PMC DOI

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closest p

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likely to be significantno p-value reported

This is most likely to be significant for the 11 cases (eight families) in which coverage of specific exons was less than 10-fold (predominantly affecting DUOXA2 and SLC5A5 ).

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