A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21.2-q21.3.

Ítems similars

• The first de novo mutation of the connexin 32 gene associated with X linked Charcot-Marie-Tooth disease.
  per: Meggouh, F, et al.
  Publicat: (1998)
• 4q21.2q21.3 Duplication: Molecular and Neuropsychological Aspects
  per: Iourov, Ivan Y., et al.
  Publicat: (2018)
• Mutations in MTMR13, a New Pseudophosphatase Homologue of MTMR2 and Sbf1, in Two Families with an Autosomal Recessive Demyelinating Form of Charcot-Marie-Tooth Disease Associated with Early-Onset Glaucoma
  per: Azzedine, H., et al.
  Publicat: (2003)
• Mutation in the epsilon subunit of the cytosolic chaperonin‐containing t‐complex peptide‐1 (Cct5) gene causes autosomal recessive mutilating sensory neuropathy with spastic paraplegia
  per: Bouhouche, A, et al.
  Publicat: (2006)
• Deletion (12)(q15q21.2).
  per: Watson, M S, et al.
  Publicat: (1989)