Abnormal expression of laminin suggests disturbance of sarcolemma-extracellular matrix interaction in Japanese patients with autosomal recessive muscular dystrophy deficient in adhalin.

Lignende værker

• Adhalin gene mutations in patients with autosomal recessive childhood onset muscular dystrophy with adhalin deficiency.
  af: Kawai, H, et al.
  Udgivet: (1995)
• Autosomal recessive oculopharyngeal muscular dystrophy.
  af: Fried, K, et al.
  Udgivet: (1975)
• Autosomal recessive limb-girdle muscular dystrophies in the Czech Republic
  af: Stehlíková, Kristýna, et al.
  Udgivet: (2014)
• Therapeutic possibilities in the autosomal recessive limb-girdle muscular dystrophies
  af: Straub, Volker, et al.
  Udgivet: (2008)
• Robust genotyping tool for autosomal recessive type of limb-girdle muscular dystrophies
  af: Inashkina, Inna, et al.
  Udgivet: (2016)