Two common mutations (p.Gln832X and c.663+1G>C) account for about a third of the DYSF mutations in Korean patients with dysferlinopathy.
| Image |  |
|---|---|
| Description | scientific article published on 31 January 2012 |
| Author/s |
author: Young-Chul Choi |
| Publication date | January 31, 2012 |
| Language | |
| Country of origin | |
| Wikipedia link | |
| Copyright status | |
| Missing/wrong data? | Edit Wikidata item |