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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2011 | 1 |
2014 | 1 |
2016 | 2 |
2017 | 1 |
2019 | 1 |
2020 | 1 |
2024 | 0 |
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Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype.
Circ Cardiovasc Genet. 2011 Aug 1;4(4):367-74. doi: 10.1161/CIRCGENETICS.110.959270. Epub 2011 May 6.
Circ Cardiovasc Genet. 2011.
PMID: 21551322
Distinguishing hypertrophic cardiomyopathy-associated mutations from background genetic noise.
Kapplinger JD, Landstrom AP, Bos JM, Salisbury BA, Callis TE, Ackerman MJ.
Kapplinger JD, et al.
J Cardiovasc Transl Res. 2014 Apr;7(3):347-61. doi: 10.1007/s12265-014-9542-z. Epub 2014 Feb 8.
J Cardiovasc Transl Res. 2014.
PMID: 24510615
Free PMC article.
Item in Clipboard
Next Generation Sequencing and Linkage Analysis for the Molecular Diagnosis of a Novel Overlapping Syndrome Characterized by Hypertrophic Cardiomyopathy and Typical Electrical Instability of Brugada Syndrome.
Mango R, Luchetti A, Sangiuolo R, Ferradini V, Briglia N, Giardina E, Ferrè F, Helmer Citterich M, Romeo F, Novelli G, Sangiuolo F.
Mango R, et al.
Circ J. 2016;80(4):938-49. doi: 10.1253/circj.CJ-15-0685. Epub 2016 Mar 9.
Circ J. 2016.
PMID: 26960954
Free article.
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Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
Walsh R, Thomson KL, Ware JS, Funke BH, Woodley J, McGuire KJ, Mazzarotto F, Blair E, Seller A, Taylor JC, Minikel EV, Exome Aggregation Consortium, MacArthur DG, Farrall M, Cook SA, Watkins H.
Walsh R, et al.
Genet Med. 2017 Feb;19(2):192-203. doi: 10.1038/gim.2016.90. Epub 2016 Aug 17.
Genet Med. 2017.
PMID: 27532257
Free PMC article.
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Thin filament dysfunctions caused by mutations in tropomyosin Tpm3.12 and Tpm1.1.
Moraczewska J.
Moraczewska J.
J Muscle Res Cell Motil. 2020 Mar;41(1):39-53. doi: 10.1007/s10974-019-09532-y. Epub 2019 Jul 3.
J Muscle Res Cell Motil. 2020.
PMID: 31270709
Free PMC article.
Review.
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