A novel c.563 T>G, p.L189R lamin A/C mutation in identical twins with dilated cardiomyopathy
Euijae Lee, Kyung-Taek Park, Jinwoo Kang, Hyunkyung Park, Jin Joo Park, Il-Young Oh, Yeonyee E. Yoon
Korean J Intern Med. 2017;32(1):178-181. Published online 2016 Mar 8 DOI: https://doi.org/10.3904/kjim.2015.146
|
Citations to this article as recorded by
Atrial fibrillation in patients with inherited cardiomyopathies
Cynthia Yeung, Andres Enriquez, Laiden Suarez-Fuster, Adrian Baranchuk
EP Europace.2019; 21(1): 22. CrossRef Case reports of a c.475G>T, p.E159* lamin A/C mutation with a family history of conduction disorder, dilated cardiomyopathy and sudden cardiac death
Tetsuro Yokokawa, Shohei Ichimura, Naoko Hijioka, Takashi Kaneshiro, Akiomi Yoshihisa, Hiroyuki Kunii, Kazuhiko Nakazato, Takafumi Ishida, Osamu Suzuki, Seiko Ohno, Takeshi Aiba, Hiroshi Ohtani, Yasuchika Takeishi
BMC Cardiovascular Disorders.2019;[Epub] CrossRef A novel LMNA nonsense mutation causes two distinct phenotypes of cardiomyopathy with high risk of sudden cardiac death in a large five-generation family
Christina R Glöcklhofer, Johannes Steinfurt, Gerlind Franke, Anselm Hoppmann, Theresa Glantschnig, Stefanie Perez-Feliz, Svenja Alter, Judith Fischer, Michael Brunner, Peter P Rainer, Anna Köttgen, Christoph Bode, Katja E Odening
EP Europace.2018;[Epub] CrossRef
|