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Object |
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Case Reports|Journal Article |
| endingPage |
285 |
| issn |
1769-7212 |
| issueIdentifier |
4 |
| pageRange |
282-285 |
| publicationName |
European Journal of Medical Genetics |
| startingPage |
282 |
| bibliographicCitation |
Mangum KD, Ferns SJ. A novel familial truncating mutation in the filamin C gene associated with cardiac arrhythmias. European Journal of Medical Genetics. 2019 Apr;62(4):282–5. doi: 10.1016/j.ejmg.2018.08.006. |
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http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_1437ad56805e94cd72d3ad1678b4817b |
| date |
201904 |
| identifier |
https://doi.org/10.1016/j.ejmg.2018.08.006
https://pubmed.ncbi.nlm.nih.gov/30118858 |
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https://portal.issn.org/resource/ISSN/1769-7212
http://rdf.ncbi.nlm.nih.gov/pubchem/journal/32436 |
| language |
English |
| source |
https://pubmed.ncbi.nlm.nih.gov/
https://www.crossref.org/ |
| title |
A novel familial truncating mutation in the filamin C gene associated with cardiac arrhythmias |
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