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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.
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
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PubType: Academic Journal
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  Data: 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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  Data: <searchLink fieldCode="AR" term="%22Genc%2C+H%2E+Maras%22">Genc, H. Maras</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Ardicli%2C+D%2E%22">Ardicli, D.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Haliloglu%2C+G%2E%22">Haliloglu, G.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Talim%2C+B%2E%22">Talim, B.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Alikasifoglu%2C+M%2E%22">Alikasifoglu, M.</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Topaloglu%2C+H%2E%22">Topaloglu, H.</searchLink><relatesTo>2</relatesTo>
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  Data: <searchLink fieldCode="JN" term="%22Neuromuscular+Disorders%22">Neuromuscular Disorders</searchLink>. Oct2016 Supplement 2, Vol. 26, pS138-S139. 1p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=118028937
RecordInfo BibRecord:
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      – Type: doi
        Value: 10.1016/j.nmd.2016.06.192
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      – Code: eng
        Text: English
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        StartPage: S138
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      – TitleFull: 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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            NameFull: Alikasifoglu, M.
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              Text: Oct2016 Supplement 2
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              Y: 2016
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