Hypoparathyroidism, deafness, and renal dysplasia syndrome: 20 Years after the identification of the first GATA3 mutations

Lemos, Manuel C. ; Thakker, Rajesh V.

Human mutation, 2020-08, Vol.41 (8), p.1341-1350 [Periódico revisado por pares]

United States: Hindawi Limited

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