https://www.selleckchem.com/products/cx-5461.html
The special clinical phenotypes shown by the two children harboring novel CHD7 variants have further expanded the phenotypic spectrum of CHARGE syndrome. The special clinical phenotypes shown by the two children harboring novel CHD7 variants have further expanded the phenotypic spectrum of CHARGE syndrome. To explore the genetic basis of a Chinese pedigree affected with Becker muscular dystrophy (BMD) with myalgia as the main feature. Clinical data of the patients and results of auxiliary examinations were retrospectively analyzed. Mult
Curtir
Comentario
Compartilhar
