Epidermolysis bullosa simplex with muscular dystrophy associated with PLEC deletion mutation

Benzer Materyaller

• A homozygous nonsense mutation in the PLEC1 gene in patients with epidermolysis bullosa simplex with muscular dystrophy.
  Yazar:: Chavanas, S, ve diğerleri
  Baskı/Yayın Bilgisi: (1996)
• Downstream effects of plectin mutations in epidermolysis bullosa simplex with muscular dystrophy
  Yazar:: Winter, Lilli, ve diğerleri
  Baskı/Yayın Bilgisi: (2016)
• Defective expression of plectin/HD1 in epidermolysis bullosa simplex with muscular dystrophy.
  Yazar:: Gache, Y, ve diğerleri
  Baskı/Yayın Bilgisi: (1996)
• Epidermolysis bullosa simplex with muscular dystrophy. Review of the literature and a case report
  Yazar:: Kyrova, Jana, ve diğerleri
  Baskı/Yayın Bilgisi: (2016)
• Plectin Deficiency Leads to Both Muscular Dystrophy and Pyloric Atresia in Epidermolysis Bullosa Simplex
  Yazar:: Natsuga, Ken, ve diğerleri
  Baskı/Yayın Bilgisi: (2010)