Growth hormone deficiency in a child with benign hereditary chorea caused by a de novo mutation of the TITF1/NKX2-1 gene-MedSci.cn

Growth hormone deficiency in a child with benign hereditary chorea caused by a de novo mutation of the TITF1/NKX2-1 gene

Trevisani, V; Predieri, B; Madeo, SF; Fusco, C; Garavelli, L; Caraffi, S; Iughetti, L

Iughetti, L (通讯作者)，Univ Modena & Reggio Emilia, Post Grad Sch Pediat Children & Adults, Dept Med & Surg Sci Mothers, Largo Pozzo 71, I-41124 Modena, Italy.;Iughetti, L (通讯作者)，Univ Modena & Reggio Emilia, Dept Med & Surg Sci Mothers, Pediat Unit, Children & Adults, Largo Pozzo 71, I-41124 Modena, Italy.

Abstract

Objectives Benign Hereditary Chorea (BHC) (MIM 118700) is a rare childhood-onset movements disorder characterized by non-progressive chorea. It is usu......

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Growth hormone deficiency in a child with benign hereditary chorea caused by a de novo mutation of the TITF1/NKX2-1 gene

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