Clinical and genetic characteristics of autosomal recessive axonal neuropathy with neuromyotonia in Russian patients

Samankaltaisia teoksia

• New allelic variant of autosomal recessive hereditary motor and sensory neuropathy type 2S resulted from mutations in gene IGHMBP2
  Tekijä: E. L. Dadali, et al.
  Julkaistu: (2016-07-01)
• AUTOSOMAL RECESSIVE PERIPHERAL NEUROPATHY WITH NEUROMYOTONIA (ARAN-NM): DESCRIPTION OF A CLINICAL CASE CONFIRMED BY A MUTATION IN THE HINT1 GENE
  Tekijä: Olga A. Klochkova, et al.
  Julkaistu: (2017-09-01)
• Spectrum of sonographic changes in hereditary motor and sensory neuropathy with autosomal dominant and X-linked inheritance
  Tekijä: E. S. Naumova, et al.
  Julkaistu: (2016-07-01)
• A case of hereditary motor and sensory neuropathy type IVA with unusual genealogy
  Tekijä: S. A. Kurbatov, et al.
  Julkaistu: (2018-07-01)
• Association of SORD mutation with autosomal recessive asymmetric distal hereditary motor neuropathy
  Tekijä: Majed Alluqmani, et al.
  Julkaistu: (2022-04-01)