Mutations in the COL5A1 gene are causal in the Ehlers-Danlos syndromes I and II.

Samankaltaisia teoksia

• Classical Ehlers-Danlos Syndrome Caused by a Mutation in Type I Collagen
  Tekijä: Nuytinck, Lieve, et al.
  Julkaistu: (2000)
• A single base mutation in COL5A2 causes Ehlers-Danlos syndrome type II.
  Tekijä: Richards, A J, et al.
  Julkaistu: (1998)
• A novel missense mutation of COL5A2 in a patient with Ehlers–Danlos syndrome
  Tekijä: Watanabe, Miki, et al.
  Julkaistu: (2016)
• Compound phenotype of osteogenesis imperfecta and Ehlers–Danlos syndrome caused by combined mutations in COL1A1 and COL5A1
  Tekijä: Lin, Zejia, et al.
  Julkaistu: (2019)
• An exon skipping mutation of a type V collagen gene (COL5A1) in Ehlers-Danlos syndrome.
  Tekijä: Nicholls, A C, et al.
  Julkaistu: (1996)