Clinical and genetic spectrum of sarcoglycanopathies in a large cohort of Chinese patients

Sarcoglycanopathies comprise four subtypes of autosomal recessive limb-girdle muscular dystrophy (LGMD2C, LGMD2D, LGMD2E, and LGMD2F) that are caused, respectively, by mutations in the SGCG, SGCA, SGCB, and SGCD ...

Source: Orphanet Journal of Rare Diseases - February 14, 2019 Category: Internal Medicine Authors: Zhiying Xie, Yue Hou, Meng Yu, Yilin Liu, Yanbin Fan, Wei Zhang, Zhaoxia Wang, Hui Xiong and Yun Yuan Tags: Research Source Type: research