The heart in m.3243A>G carriers
Author:
Funder
none
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine
Link
http://link.springer.com/content/pdf/10.1007/s00059-018-4739-6.pdf
Reference41 articles.
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2. El-Hattab AW, Adesina AM, Jones J, Scaglia F (2015) MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options. Mol Genet Metab 116:4–12
3. de Laat P, Janssen MC, Alston CL, Taylor RW, Rodenburg RJ, Smeitink JA (2016) Three families with ‘de novo’ m.3243 A〉G mutation. Bba Clin 6:19–24
4. Vydt TC, de Coo RF, Soliman OI, Ten Cate FJ, van Geuns RJ, Vletter WB, Schoonderwoerd K, van den Bosch BJ, Smeets HJ, Geleijnse ML (2007) Cardiac involvement in adults with m.3243A〉G MELAS gene mutation. Am J Cardiol 99:264–269
5. Gál A, Szabó A, Pentelényi K, Pál Z (2008) Maternally inherited diabetes mellitus, deafness, chronic progressive external ophthalmoplegia and myopathy as the result of A3243G mutation of mtDNA. Orv Hetil 149:1593–1598
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