Related Articles

• α-actin gene mutations and polymorphisms in Italian patients with nemaline myopathy
• An examination of the regulatory mechanism of Pxdn mutation-induced eye disorders using microarray analysis
• Identification of novel mutations including a double mutation in patients with inherited cardiomyopathy by a targeted sequencing approach using the Ion Torrent PGM system
• Clinical and pathological features of patients with nemaline myopathy
• Use of RNA‑sequencing to detect abnormal transcription of the collagen α‑2 (VI) chain gene that can lead to Bethlem myopathy