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Year | Number of Results |
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2003 | 1 |
2004 | 1 |
2005 | 2 |
2012 | 1 |
2024 | 0 |
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Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy.
Circulation. 2003 Jul 29;108(4):445-51. doi: 10.1161/01.CIR.0000080896.52003.DF. Epub 2003 Jul 14.
Circulation. 2003.
PMID: 12860912
Cardiac troponin I mutations in Australian families with hypertrophic cardiomyopathy: clinical, genetic and functional consequences.
Doolan A, Tebo M, Ingles J, Nguyen L, Tsoutsman T, Lam L, Chiu C, Chung J, Weintraub RG, Semsarian C.
Doolan A, et al.
J Mol Cell Cardiol. 2005 Feb;38(2):387-93. doi: 10.1016/j.yjmcc.2004.12.006. Epub 2005 Jan 27.
J Mol Cell Cardiol. 2005.
PMID: 15698845
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Frequency and clinical expression of cardiac troponin I mutations in 748 consecutive families with hypertrophic cardiomyopathy.
Mogensen J, Murphy RT, Kubo T, Bahl A, Moon JC, Klausen IC, Elliott PM, McKenna WJ.
Mogensen J, et al.
J Am Coll Cardiol. 2004 Dec 21;44(12):2315-25. doi: 10.1016/j.jacc.2004.05.088.
J Am Coll Cardiol. 2004.
PMID: 15607392
Free article.
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Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling.
Ingles J, Doolan A, Chiu C, Seidman J, Seidman C, Semsarian C.
Ingles J, et al.
J Med Genet. 2005 Oct;42(10):e59. doi: 10.1136/jmg.2005.033886.
J Med Genet. 2005.
PMID: 16199542
Free PMC article.
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High prevalence of Arginine to Glutamine substitution at 98, 141 and 162 positions in Troponin I (TNNI3) associated with hypertrophic cardiomyopathy among Indians.
Rani DS, Nallari P, Priyamvada S, Narasimhan C, Singh L, Thangaraj K.
Rani DS, et al.
BMC Med Genet. 2012 Aug 10;13:69. doi: 10.1186/1471-2350-13-69.
BMC Med Genet. 2012.
PMID: 22876777
Free PMC article.
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