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Year | Number of Results |
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2017 | 1 |
2018 | 1 |
2020 | 1 |
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Mutations in the LMNA gene encoding lamin A/C.
Hum Mutat. 2000 Dec;16(6):451-9. doi: 10.1002/1098-1004(200012)16:6<451::AID-HUMU1>3.0.CO;2-9.
Hum Mutat. 2000.
PMID: 11102973
Review.
Integrated analysis reveals the alterations that LMNA interacts with euchromatin in LMNA mutation-associated dilated cardiomyopathy.
Zhang X, Shao X, Zhang R, Zhu R, Feng R.
Zhang X, et al.
Clin Epigenetics. 2021 Jan 6;13(1):3. doi: 10.1186/s13148-020-00996-1.
Clin Epigenetics. 2021.
PMID: 33407844
Free PMC article.
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LMNA Missense Mutation Causes Nonsense-Mediated mRNA Decay and Severe Dilated Cardiomyopathy.
Kato K, Ohno S, Sonoda K, Fukuyama M, Makiyama T, Ozawa T, Horie M.
Kato K, et al.
Circ Genom Precis Med. 2020 Oct;13(5):435-443. doi: 10.1161/CIRCGEN.119.002853. Epub 2020 Aug 20.
Circ Genom Precis Med. 2020.
PMID: 32818388
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Inherited dilated cardiomyopathy in a large Moroccan family caused by LMNA mutation.
Adadi N, Radi FZ, Lahrouchi N, Hara L, Ratbi I, Elalaoui SC, Alders M, Zarzur J, Bezzina C, Sefiani A.
Adadi N, et al.
Anatol J Cardiol. 2018 Jul;20(1):65-68. doi: 10.14744/AnatolJCardiol.2018.69639.
Anatol J Cardiol. 2018.
PMID: 29952368
Free PMC article.
No abstract available.
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Gene-Based Risk Stratification for Cardiac Disorders in LMNA Mutation Carriers.
Nishiuchi S, Makiyama T, Aiba T, Nakajima K, Hirose S, Kohjitani H, Yamamoto Y, Harita T, Hayano M, Wuriyanghai Y, Chen J, Sasaki K, Yagihara N, Ishikawa T, Onoue K, Murakoshi N, Watanabe I, Ohkubo K, Watanabe H, Ohno S, Doi T, Shizuta S, Minamino T, Saito Y, Oginosawa Y, Nogami A, Aonuma K, Kusano K, Makita N, Shimizu W, Horie M, Kimura T.
Nishiuchi S, et al.
Circ Cardiovasc Genet. 2017 Dec;10(6):e001603. doi: 10.1161/CIRCGENETICS.116.001603.
Circ Cardiovasc Genet. 2017.
PMID: 29237675
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