DUOX2/DUOXA2 mutations frequently cause congenital...

Thyroid 2019 / 05

DUOX2/DUOXA2 mutations frequently cause congenital hypothyroidism which evades detection on UK newborn screening

Peters, Catherine, Nicholas, Adeline K., Schoenmakers, Erik, Lyons, Greta, Langham, Shirley, Serra, Eva G., Sebire, Neil J., Muzza, Marina, Fugazzola, Laura, Schoenmakers, Nadia
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Journal:
Thyroid
DOI:
10.1089/thy.2018.0587
Date:
May, 2019
File:
PDF, 1.05 MB
2019
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