Type I membranous anomaly in Stickler syndrome

Ophthalmic Genet. 2018 Jan-Feb;39(1):147. doi: 10.1080/13816810.2017.1326510. Epub 2017 May 30.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Arthritis
  • Collagen Type II / genetics
  • Connective Tissue Diseases*
  • Hearing Loss, Sensorineural
  • Humans
  • Mutation
  • Pedigree
  • Retinal Detachment*

Substances

  • Collagen Type II

Supplementary concepts

  • Stickler syndrome, type 1