Phenotypic high myopia in X-linked retinitis pigmentosa secondary to a novel mutation in the RPGR gene. [electronic resource]
Producer: 20200313Description: 170-176 p. digitalISSN:- 1744-5094
- Adult
- Aged
- Child
- DNA Mutational Analysis
- Electroretinography
- Exons -- genetics
- Eye Proteins -- genetics
- Female
- Genetic Association Studies
- Genetic Diseases, X-Linked -- diagnosis
- Heterozygote
- Humans
- Male
- Middle Aged
- Mutation
- Myopia, Degenerative -- diagnosis
- Pedigree
- Phenotype
- Retinitis Pigmentosa -- diagnosis
- Visual Field Tests
- Visual Fields -- physiology
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Publication Type: Case Reports; Journal Article
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