Autosomal dominant axonal Charcot-Marie-Tooth disease type 2 (CMT2G) maps to chromosome 12q12–q13.3

Gelijkaardige items

• Homozygosity mapping of autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy (CMT4H) to a novel locus on chromosome 12p11.21-q13.11
  door: Sandre-Giovannoli, A, et al.
  Gepubliceerd in: (2005)
• Assignment of the Charcot-Marie-Tooth neuropathy type 1 (CMT 1a) gene to 17p11.2-p12.
  door: Timmerman, V, et al.
  Gepubliceerd in: (1990)
• Genetics of Charcot-Marie-Tooth (CMT) Disease within the Frame of the Human Genome Project Success
  door: Timmerman, Vincent, et al.
  Gepubliceerd in: (2014)
• Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research Group.
  door: Raeymaekers, P, et al.
  Gepubliceerd in: (1992)
• A Second Locus for an Axonal Form of Autosomal Recessive Charcot-Marie-Tooth Disease Maps to Chromosome 19q13.3
  door: Leal, Alejandro, et al.
  Gepubliceerd in: (2001)