Limb girdle muscular dystrophy 23 caused by compound heterozygous mutations of LAMA2 gene

• Main Authors: Yuqing Xu (Author), Linyan Zhu (Author), Yeqing Qian (Author), Minyue Dong (Author)
• פורמט: ספר
• יצא לאור: Frontiers Media S.A., 2023-06-01T00:00:00Z.
• נושאים: article
• גישה מקוונת: Connect to this object online.

IntroductionMutations of LAMA2 gene are associated with congenital muscular dystrophy (CMD). The LAMA2-related CMD mainly consists of two diseases, merosin deficient congenital muscular dystrophies type 1A (MDC1A) and limb girdle muscular dystrophy 23 (LGMD23). LGMD23 is characterized by slowly prog...