THE CLINICAL AND MOLECULAR CHARACTERIZATION OF PATIENTS WITH DYSHORMONOGENIC CONGENITAL HYPOTHYROIDISM REVEALS SPECIFIC DIAGNOSTIC CLUES FOR DUOX2 DEFECTS
Muzza, M, Rabbiosi, S, Vigone, MC, Zamproni, I, Cirello, V, Maffini, MA, Maruca, K, Schoenmakers, N, Beccaria, L, Gallo, F, Park, S-M, Beck-Peccoz, P, Persani, L, Weber, G, Fugazzola, LLanguage:
english
Journal:
The Journal of Clinical Endocrinology & Metabolism
DOI:
10.1210/jc.2013-3618
Date:
January, 2013
File:
PDF, 735 KB
english, 2013
File converter
More search results
More benefits 
