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Characterization of a novel loss-of-function mutation of PAX8 associated with congenital hypothyroidism

✍ Scribed by Tina Di Palma; Emilia Zampella; Maria Grazia Filippone; Paolo Emidio Macchia; Carrie Ris-Stalpers; Monique De Vroede; Mariastella Zannini


Book ID
108704716
Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
225 KB
Volume
73
Category
Article
ISSN
0300-0664

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