Clinical features and genotypes of Laing distal myopathy in a group of Chinese patients, with in-frame deletions of MYH7 as common mutations.
Meng YuYing ZhuYuanyuan LuHe LvWei ZhangYun YuanZhaoxia WangPublished in: Orphanet journal of rare diseases (2020)
Our study further expanded the phenotypes and genotypes of Laing distal myopathy. In-frame deletions of the MYH7 gene are common causes of Laing distal myopathy.