Article

Mutational screening of the TPO and DUOX2 genes in Argentinian children with congenital hypothyroidism due to thyroid dyshormonogenesis.

2022-01-13

Abstract excerpt

<title>Abstract</title> <p>Purpose Primary congenital hypothyroidism (CH) is the most common endocrine disease in children and one of the preventable causes of both cognitive and motor deficits. We present a genetic and bioinformatics investigation of rational clinical design in 16 Argentine patients suspected of CH due to thyroid dyshormonogenesis (TDH). Methods Next-Generation Sequencing approach was used to...

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Literature Corpus work: 4ac0c919-eb60-59d1-bb17-e92c62ac15c7
DOI: 10.21203/rs.3.rs-1239485/v1

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