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  • Christopher Todd Meredith, Ralf Herrmann, +16 authors Nigel G. Laing
  • Biology, Medicine
  • American journal of human genetics
  • 2004 (First Publication: 1 October 2004)
  • We previously linked Laing-type early-onset autosomal dominant distal myopathy (MPD1) to a 22-cM region of chromosome 14. One candidate gene in the region, MYH7, which is mutated in cardiomyopathyExpand
  • Maria Tsaousidou, Karim Ouahchi, +12 authors Andrew H. Crosby
  • Biology, Medicine
  • American journal of human genetics
  • 2008 (First Publication: 8 February 2008)
  • The hereditary spastic paraplegias (HSPs) are a genetically and clinically heterogeneous group of upper-motor-neuron degenerative diseases characterized by selective axonal loss in the corticospinalExpand