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.
Authors
Philip Alexander
1
,
Arabella Poulson
1
,
Annie McNinch
1
,
Allan Richards
1
,
Martin Snead
1
Affiliation
1
a NHS England National Stickler Diagnostic Service , Cambridge University Hospitals NHS Foundation Trust , Cambridge , UK.
PMID:
28557656
DOI:
10.1080/13816810.2017.1326510
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