Spectrum of Mutations in Hypertrophic Cardiomyopathy Genes Among Tunisian Patients

Hypertrophic cardiomyopathy (HCM) is a common cardiac genetic disorder associated with heart failure and sudden death. Mutations in the cardiac sarcomere genes are found in approximately half of HCM patients and are more common among cases with a family history of the disease. Data about the mutatio...

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Veröffentlicht in:Genetic testing and molecular biomarkers 2016-11, Vol.20 (11), p.674-679
Hauptverfasser: Jaafar, Nawel, Gómez, Juan, Kammoun, Ikram, Zairi, Ihsen, Amara, Wael Ben, Kachboura, Salem, Kraiem, Sondes, Hammami, Mohamed, Iglesias, Sara, Alonso, Belén, Coto, Eliecer
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Sprache:eng
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