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

Podobne zapisy

• Homozygosity mapping of autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy (CMT4H) to a novel locus on chromosome 12p11.21-q13.11
  od: Sandre-Giovannoli, A, i wsp.
  Wydane: (2005)
• Assignment of the Charcot-Marie-Tooth neuropathy type 1 (CMT 1a) gene to 17p11.2-p12.
  od: Timmerman, V, i wsp.
  Wydane: (1990)
• Genetics of Charcot-Marie-Tooth (CMT) Disease within the Frame of the Human Genome Project Success
  od: Timmerman, Vincent, i wsp.
  Wydane: (2014)
• Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research Group.
  od: Raeymaekers, P, i wsp.
  Wydane: (1992)
• Localization of the Gene for the Intermediate Form of Charcot-Marie-Tooth to Chromosome 10q24.1-q25.1
  od: Verhoeven, Kristien, i wsp.
  Wydane: (2001)