论文信息 - A novel NKX2.1 mutation in a family with hypothyroidism and benign hereditary chorea. - 字舞流文

A novel NKX2.1 mutation in a family with hypothyroidism and benign hereditary chorea.

P. Macchia | G. De Michele | A. Filla | G. Fenzi | E. Salvatore | E. Zampella | G. Rossi | A. Ferrara | S. Capuano | L. Di Maio | Giuseppina Del Prete | A. M. Ferrara