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 | AVESİS

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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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Genc H. M., Ardicli D., Haliloglu G., Talim B., Alikasifoglu M., Topaloglu H.

21st International Congress of the World-Muscle-Society, Granada, Nicaragua, 4 - 08 October 2016, vol.26

Publication Type: Conference Paper / Summary Text
Volume: 26
Doi Number: 10.1016/j.nmd.2016.06.192
City: Granada
Country: Nicaragua
Hacettepe University Affiliated: Yes