The uncommon occurrence of two common inherited disorders in a single patient: a mini case series. [electronic resource]
Producer: 20190410Description: 631-636 p. digitalISSN:- 1744-5094
- ATP-Binding Cassette Transporters -- genetics
- Adolescent
- Aged
- Arthritis -- complications
- Collagen Type XI -- genetics
- Connective Tissue Diseases -- complications
- Eye Diseases, Hereditary -- complications
- Female
- Hearing Loss, Sensorineural -- complications
- Humans
- Macular Degeneration -- complications
- Male
- Mutation
- Prognosis
- Retinal Detachment -- complications
- Stargardt Disease
No physical items for this record
Publication Type: Case Reports; Journal Article
There are no comments on this title.
Log in to your account to post a comment.