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

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

doi:10.1016/j.nmd.2016.06.192

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

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

SB Ankara Children's Hematology Oncology Training and Research Hospital
Hacettepe University

Research output: Contribution to journal › Meeting Abstract › peer-review

Original language	English
Pages (from-to)	S138-S139
Number of pages	2
Journal	Neuromuscular Disorders
Volume	26
DOIs	https://doi.org/10.1016/j.nmd.2016.06.192
Publication status	Published - Oct 2016
Event	21st International Congress of the World-Muscle-Society - Granada, Spain Duration: 4 Oct 2016 → 8 Oct 2016

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10.1016/j.nmd.2016.06.192

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@article{0977d99f36164c0cb586b051e98c21ce,

title = "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",

author = "Genc, \{H. Maras\} and D. Ardicli and G. Haliloglu and B. Talim and M. Alikasifoglu and H. Topaloglu",

year = "2016",

month = oct,

doi = "10.1016/j.nmd.2016.06.192",

language = "English",

volume = "26",

pages = "S138--S139",

journal = "Neuromuscular Disorders",

issn = "0960-8966",

publisher = "Elsevier Ltd",

note = "21st International Congress of the World-Muscle-Society ; Conference date: 04-10-2016 Through 08-10-2016",

}

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. / Genc, H. Maras; Ardicli, D.; Haliloglu, G. et al.
In: Neuromuscular Disorders, Vol. 26, 10.2016, p. S138-S139.

Research output: Contribution to journal › Meeting Abstract › peer-review

TY - JOUR

T1 - Solving a puzzle

T2 - 21st International Congress of the World-Muscle-Society

AU - Genc, H. Maras

AU - Ardicli, D.

AU - Haliloglu, G.

AU - Talim, B.

AU - Alikasifoglu, M.

AU - Topaloglu, H.

PY - 2016/10

Y1 - 2016/10

UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=performanshacettepe&SrcAuth=WosAPI&KeyUT=WOS:000384790100182&DestLinkType=FullRecord&DestApp=WOS_CPL

U2 - 10.1016/j.nmd.2016.06.192

DO - 10.1016/j.nmd.2016.06.192

M3 - Meeting Abstract

SN - 0960-8966

VL - 26

SP - S138-S139

JO - Neuromuscular Disorders

JF - Neuromuscular Disorders

Y2 - 4 October 2016 through 8 October 2016

ER -

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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