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Identification and characterization of four PAX8 rare sequence variants (p.T225M, p.L233L, p.G336S and p.A439A) in patients with congenital hypothyroidism and dysgenetic thyroid glands

✍ Scribed by Sebastián A. Esperante; Carina M. Rivolta; Lucrecia Miravalle; Viviana Herzovich; Sonia Iorcansky; Marco Baralle; Héctor M. Targovnik


Book ID
108703992
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
280 KB
Volume
68
Category
Article
ISSN
0300-0664

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