Two common mutations (p.Gln832X and c.663+1G>C) account for about a third of the DYSF mutations in Korean patients with dysferlinopathy. (Q53389267)
Jump to navigation
Jump to search
scientific article published on 31 January 2012
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Two common mutations (p.Gln832X and c.663+1G>C) account for about a third of the DYSF mutations in Korean patients with dysferlinopathy. |
scientific article published on 31 January 2012 |
Statements
Two common mutations (p.Gln832X and c.663+1G>C) account for about a third of the DYSF mutations in Korean patients with dysferlinopathy (English)
Young-Eun Park
Hyang-Sook Kim
Chang-Hoon Lee
Tai-Seung Nam