Deletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin α2-related muscular dystrophy
LAMA2基因第4外显子缺失是中国层粘连蛋白α2相关肌营养不良症患者中最常见的突变。
期刊:Scientific Reports
影响因子:3.8
doi:10.1038/s41598-018-33098-3.
Lin Ge,Aijie Liu,Kai Gao,Renqian Du,Juan Ding,Bing Mao,Ying Hua,Xiaoli Zhang,Dandan Tan,Haipo Yang,Xiaona Fu,Yanbin Fan,Ling Zhang,Shujuan Song,Jian Wu,Feng Zhang,Yuwu Jiang,Xiru Wu,Hui Xiong
