Identification of mutations in the arginine vasopressin receptor 2 gene causing nephrogenic diabetes insipidus in Chinese patients

スポンサーリンク

概要

著者

関連論文

Genetic studies on SURF1 mutations in Chinese patients with mitochondrial encephalopathy
A Clinical Survey of 65 Patients with Leigh Syndrome
SCN1A, SCN1B, and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plus
Histomorphometric study in children with idiopathic nephrotic syndrome
A clinicopathological study of idiopathic nephrotic syndrome in children
Identification of mutations in the arginine vasopressin receptor 2 gene causing nephrogenic diabetes insipidus in Chinese patients
Mutation spectrum of and founder effects affecting the PTS gene in East Asian populations
Analysis of SCN1A mutation and parental origin in patients with Dravet syndrome
Mutation spectrum of MMACHC in Chinese patients with combined methylmalonic aciduria and homocystinuria
Clinical analysis of five infants with glycogen storage disease of the heart-Pompe's disease.

スポンサーリンク