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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1958 1
1961 1
1963 1
1964 1
1965 1
1966 1
1967 1
1968 1
1973 3
1974 1
1975 1
1976 2
1977 1
1979 3
1980 1
1981 1
1982 3
1983 2
1985 3
1986 1
1987 5
1988 1
1989 4
1990 7
1991 2
1992 7
1993 4
1994 5
1995 4
1996 4
1997 3
1998 3
1999 6
2000 7
2001 5
2002 3
2003 8
2004 3
2005 4
2024 0

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PubMed (OMIM) for id: 501195

115 results

Results by year

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Page 1
Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause laing early-onset distal myopathy (MPD1).
Meredith C, Herrmann R, Parry C, Liyanage K, Dye DE, Durling HJ, Duff RM, Beckman K, de Visser M, van der Graaff MM, Hedera P, Fink JK, Petty EM, Lamont P, Fabian V, Bridges L, Voit T, Mastaglia FL, Laing NG. Meredith C, et al. Am J Hum Genet. 2004 Oct;75(4):703-8. doi: 10.1086/424760. Epub 2004 Aug 20. Am J Hum Genet. 2004. PMID: 15322983 Free PMC article.
Aldosterone, through novel signaling proteins, is a fundamental molecular bridge between the genetic defect and the cardiac phenotype of hypertrophic cardiomyopathy.
Tsybouleva N, Zhang L, Chen S, Patel R, Lutucuta S, Nemoto S, DeFreitas G, Entman M, Carabello BA, Roberts R, Marian AJ. Tsybouleva N, et al. Circulation. 2004 Mar 16;109(10):1284-91. doi: 10.1161/01.CIR.0000121426.43044.2B. Epub 2004 Mar 1. Circulation. 2004. PMID: 14993121 Free PMC article.
115 results