Late onset CMT2A in a Family with an MFN2 Variant: c.2222T > G (p.Leu741Trp) Article

cited authors

  • Lin, Hsin-Pin; Ho, Kwo Wei David; Jerath, Nivedita U.

authors

Publication Date

  • January 1, 2019

webpage

published in

category

keywords

  • Charcot-Marie-Tooth disease
  • MFN2 protein
  • Neuromuscular diseases
  • genetic variation
  • hereditary sensory and motor neuropathy
  • human
  • pathogenicity
  • phenotype
  • type 2A

start page

  • 259

end page

  • 261

volume

  • 6

issue

  • 2