A novel mutation in the ABCR gene in four patients with autosomal recessive Stargardt disease. [electronic resource]
Producer: 19991228Description: 720-4 p. digitalISSN:- 0002-9394
- ATP-Binding Cassette Transporters -- genetics
- Adult
- Base Sequence
- Cohort Studies
- DNA Mutational Analysis
- Eye Diseases, Hereditary -- genetics
- Female
- Fluorescein Angiography
- Fundus Oculi
- Humans
- Macular Degeneration -- genetics
- Middle Aged
- Molecular Sequence Data
- Pedigree
- Point Mutation
- Polymorphism, Single-Stranded Conformational
- Sequence Analysis, DNA
- Visual Acuity
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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