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Published in 2022 at "Human Molecular Genetics"
DOI: 10.1093/hmg/ddac093
Abstract: Abstract Congenital hypothyroidism due to thyroid dysgenesis (TD), presented as thyroid aplasia, hypoplasia or ectopia, is one of the most prevalent rare diseases with an isolated organ malformation. The pathogenesis of TD is largely unknown,…
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Keywords:
thyroid dysgenesis;
locus 2q33;
risk locus;
wnt signaling ... See more keywords