Clinical phenotype in a Swedish family with a mutation in the IMPDH1 gene.
Author
Publishing year
2005
Language
English
Pages
24-119
Publication/Series
Ophthalmic Genetics
Volume
26
Issue
3
Links
Document type
Journal article
Publisher
Taylor & Francis
Topic
- Ophthalmology
Status
Published
ISBN/ISSN/Other
- ISSN: 1744-5094