Novel Nucleotide Changes in Mitochondrial COXII, Cytochrome B and tRNAGlu Genes in Patients with Brugada Syndrome
Introduction: The Brugada syndrome (BrS) belongs to cardiac arrhythmia disorders that is seen on the echocardiogram bands and is a significant cause of sudden death in young adults. At the molecular level, mechanisms that contribute to BrS are mutations in genes that encode for ion channels. It has...
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| Format: | Artigo |
| Sprache: | Persa |
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Shahid Sadoughi University of Medical Sciences
2014-04-01
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| Schriftenreihe: | Majallah-i Dānishgāh-i ’Ulūm-i Pizishkī-i Shahīd Ṣadūqī Yazd |
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| Online-Zugang: | http://jssu.ssu.ac.ir/browse.php?a_code=A-10-1521-1&slc_lang=en&sid=1 |
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