1 | MPD1, MYH7
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| Two families with MYH7 distal myopathy associated with cardiomyopathy and core formations.
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| Naddaf E, Waclawik AJ.
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| J Clin Neuromuscul Dis 16(3):164-9. doi: 10.1097/CND.0000000000000069.
2015
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2 | MPD1, MYH7
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| Novel mutation in MYH7 gene associated with distal myopathy and cardiomyopathy.
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| Homayoun H, Khavandgar S, Hoover JM, Mohsen AW, Vockley J, Lacomis D, Clemens PR.
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| Neuromuscul Disord 21(3):219-22. Epub 2011 Jan 5. 2011
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3 | FSS, IBM3, MMS, MPD1, MYH2, MYH3, MYH7, MYH8, SHHS, TPCS
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| Thick filament diseases.
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| Oldfors A, Lamont PJ.
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| Adv Exp Med Biol 642:78-91. Review.PMID: 19181095 2008
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4 | CMH1, MMS, MPD1, MYH7
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| Symptomatic distal myopathy with cardiomyopathy due to a MYH7 mutation.
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| Overeem S, Schelhaas HJ, Blijham PJ, Grootscholten MI, ter Laak HJ, Timmermans J, van den Wijngaard A, Zwarts MJ.
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| Neuromuscul Disord 17(6):490-3. Epub 2007 Mar 23.
2007
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5 | MPD1, MYH7
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| Mutations in the Slow Skeletal Muscle Fiber Myosin Heavy Chain Gene (MYH7) Cause Laing Early-Onset Distal Myopathy (MPD1).
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| 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.
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| Am J Hum Genet 75(4):703-8. Epub 2004 Aug 20. 2004
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6 | MPD1
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| Autosomal dominant distal myopathy: further evidence of a chromosome 14 locus.
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| Voit T, Kutz P, Leube B, Neuen-Jacob E, Schroder JM, Cavallotti D, Vaccario ML, Schaper J, Broich P, Cohn R, Baethmann M, Gohlich-Ratmann G, Scoppetta C, Herrmann R.
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| Neuromuscul Disord 11(1):11-9. 2001
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7 | MPD1
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| Autosomal dominant distal myopathy : linkage to chromosome 14.
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| Laing NG, et al.
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| Am J Hum Genet 56 : 422-427. 1995
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