Homozygosity for SCN4A Arg1142Gln causes congenital myopathy with variable disease expression
Research output: Contribution to journal › Journal article › Research › peer-review
Documents
- Homozygosity-e267.full
Final published version, 409 KB, PDF document
| Original language | English |
|---|---|
| Journal | Neurology: Genetics |
| Volume | 4 |
| Issue number | 5 |
| Pages (from-to) | e267 |
| Number of pages | 3 |
| ISSN | 2376-7839 |
| DOIs | |
| Publication status | Published - Oct 2018 |
Number of downloads are based on statistics from Google Scholar and www.ku.dk
No data available
ID: 214578794