P.172 - Solving a puzzle: Incidentally detected high creatine kinase level combined with a family history of cardiomyopathy and sudden unexplained death leading to diagnosis of LMNA mutation.
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| Title: | P.172 - Solving a puzzle: Incidentally detected high creatine kinase level combined with a family history of cardiomyopathy and sudden unexplained death leading to diagnosis of LMNA mutation. |
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| Authors: | Genc, H. Maras1, Ardicli, D.2, Haliloglu, G.2, Talim, B.2, Alikasifoglu, M.3, Topaloglu, H.2 |
| Source: | Neuromuscular Disorders. Oct2016 Supplement 2, Vol. 26, pS138-S139. 1p. |
| Database: | Academic Search Ultimate |
| ISSN: | 09608966 |
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| DOI: | 10.1016/j.nmd.2016.06.192 |
