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1995 | 1 |
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The origins of hypertrophic cardiomyopathy-causing mutations in two South African subpopulations: a unique profile of both independent and founder events.
Am J Hum Genet. 1999 Nov;65(5):1308-20. doi: 10.1086/302623.
Am J Hum Genet. 1999.
PMID: 10521296
Free PMC article.
Troponin T and beta-myosin mutations have distinct cardiac functional effects in hypertrophic cardiomyopathy patients without hypertrophy.
Revera M, van der Merwe L, Heradien M, Goosen A, Corfield VA, Brink PA, Moolman-Smook JC.
Revera M, et al.
Cardiovasc Res. 2008 Mar 1;77(4):687-94. doi: 10.1093/cvr/cvm075. Epub 2007 Nov 20.
Cardiovasc Res. 2008.
PMID: 18029407
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Identification of a novel Ala797Thr mutation in exon 21 of the beta-myosin heavy chain gene in hypertrophic cardiomyopathy.
Moolman JC, Brink PA, Corfield VA.
Moolman JC, et al.
Hum Mutat. 1995;6(2):197-8. doi: 10.1002/humu.1380060219.
Hum Mutat. 1995.
PMID: 7581410
No abstract available.
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