Genetic spectrum and clinical features of PMP22 point mutations in Japanese Charcot-Marie-Tooth disease. Yano C, Ando M, Higuchi Y, Hobara T, Yuan J-H, Yoshimura A, Nagatomo R, Kojima F, Hiramatsu Y, Nozuma S, et al. J Neurol. 2026 Jun 29; 273(7). PMID: 42371158. Abstract CommentRecommendBookmarkWatch