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 |
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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 |
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ID: 214578794