Mutations in the RPGR gene cause X-linked cone dystrophy. [electronic resource]
Producer: 20020909Description: 605-11 p. digitalISSN:- 0964-6906
- Amino Acid Sequence
- Base Sequence
- Carrier Proteins -- genetics
- Color Vision Defects -- genetics
- Eye Proteins
- Glutamic Acid -- metabolism
- Heterozygote
- Humans
- Male
- Mutation -- genetics
- Open Reading Frames
- Pedigree
- Photophobia -- genetics
- Retinal Cone Photoreceptor Cells -- physiopathology
- Retinal Degeneration -- genetics
- Sequence Deletion
- Visual Fields
- X Chromosome
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.
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