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APOE is a potential modifier gene in an autosomal dominant form of frontotemporal dementia (IBMPFD).
Genet Med. 2007 Jan;9(1):9-13. doi: 10.1097/gim.0b013e31802d830d.
Genet Med. 2007.
PMID: 17224685
Free article.
Autosomal dominant inclusion body myopathy, Paget disease of bone, and frontotemporal dementia.
Kimonis VE, Watts GD.
Kimonis VE, et al.
Alzheimer Dis Assoc Disord. 2005 Oct-Dec;19 Suppl 1:S44-7. doi: 10.1097/01.wad.0000183081.76820.5a.
Alzheimer Dis Assoc Disord. 2005.
PMID: 16317258
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Clinical and genetic heterogeneity in chromosome 9p associated hereditary inclusion body myopathy: exclusion of GNE and three other candidate genes.
Watts GD, Thorne M, Kovach MJ, Pestronk A, Kimonis VE.
Watts GD, et al.
Neuromuscul Disord. 2003 Sep;13(7-8):559-67. doi: 10.1016/s0960-8966(03)00070-1.
Neuromuscul Disord. 2003.
PMID: 12921793
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Heterogeneity in familial dominant Paget disease of bone and muscular dystrophy.
Waggoner B, Kovach MJ, Winkelman M, Cai D, Khardori R, Gelber D, Kimonis VE.
Waggoner B, et al.
Am J Med Genet. 2002 Mar 15;108(3):187-91. doi: 10.1002/ajmg.10199.
Am J Med Genet. 2002.
PMID: 11891683
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