De novo insG619 mutation in PAX2 gene in a Japanese patient with papillorenal syndrome. [electronic resource]
Producer: 20050425Description: 733-5 p. digitalISSN:- 0002-9394
- Abnormalities, Multiple -- genetics
- Child, Preschool
- Coloboma -- genetics
- DNA Mutational Analysis
- DNA-Binding Proteins -- genetics
- Exons -- genetics
- Female
- Humans
- Kidney -- abnormalities
- Mutation, Missense
- Optic Disk -- abnormalities
- Optic Nerve -- abnormalities
- PAX2 Transcription Factor
- Syndrome
- Transcription Factors -- genetics
- Ultrasonography
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.