Homozygosity for SCN4A Arg1142Gln causes congenital myopathy with variable disease expression

Research output: Contribution to journalJournal articleResearchpeer-review

Documents

Christine K Sloth, Federico Denti, Nicole Schmitt, Bo Hjorth Bentzen, Christina Fagerberg, John Vissing, David Gaist

Original languageEnglish
JournalNeurology: Genetics
Volume4
Issue number5
Pages (from-to)e267
Number of pages3
ISSN2376-7839
DOIs
Publication statusPublished - Oct 2018

Number of downloads are based on statistics from Google Scholar and www.ku.dk


No data available

ID: 214578794