Study on the gene and phenotypic characterisation of autosomal recessive demyelinating motor and sensory neuropathy (Charcot-Marie-Tooth disease) with a gene locus on chromosome 5q23-q33

Samankaltaisia teoksia

• A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21.2-q21.3.
  Tekijä: Bouhouche, A, et al.
  Julkaistu: (1999)
• Autosomal recessive Charcot-Marie-Tooth disease
  Tekijä: MALCOLM, S
  Julkaistu: (1999)
• PLEKHG5 deficiency leads to an intermediate form of autosomal-recessive Charcot–Marie–Tooth disease
  Tekijä: Azzedine, Hamid, et al.
  Julkaistu: (2013)
• Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease
  Tekijä: Kim, Hyeon Jin, et al.
  Julkaistu: (2013)
• 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
  Tekijä: Azzedine, H., et al.
  Julkaistu: (2003)