Two common mutations (p.Gln832X and c.663+1G>C) account for about a third of the DYSF mutations in Korean patients with dysferlinopathy

Young Eun Park, Hyang Sook Kim, Chang Hoon Lee, Tai Seung Nam, Young Chul Choi, Dae Seong Kim

Research output: Contribution to journalArticle

10 Citations (Scopus)

Fingerprint Dive into the research topics of 'Two common mutations (p.Gln832X and c.663+1G>C) account for about a third of the DYSF mutations in Korean patients with dysferlinopathy'. Together they form a unique fingerprint.

Medicine & Life Sciences