Dominant hereditary inclusion-body myopathy gene (IBM3) maps to chromosome region 17p13.1.

Lignende værker

• Autosomal dominant myopathy: Missense mutation (Glu-706 → Lys) in the myosin heavy chain IIa gene
  af: Martinsson, Tommy, et al.
  Udgivet: (2000)
• Hereditary Inclusion Body Myopathy (HIBM2)
  af: Jay, Chris M., et al.
  Udgivet: (2009)
• The Proteomic Profile of Hereditary Inclusion Body Myopathy
  af: Sela, Ilan, et al.
  Udgivet: (2011)
• Clinical Delineation and Localization to Chromosome 9p13.3–p12 of a Unique Dominant Disorder in Four Families: Hereditary Inclusion Body Myopathy, Paget Disease of Bone, and Frontotemporal Dementia
  af: Kovach, Margaret J., et al.
  Udgivet: (2001)
• A Locus for Autosomal Dominant “Pure” Hereditary Spastic Paraplegia Maps to Chromosome 19q13
  af: Reid, E., et al.
  Udgivet: (2000)