A novel 7 bp deletion in PRPF31 associated with autosomal dominant retinitis pigmentosa with incomplete penetrance in an Indian family (Q56988670)
Jump to navigation
Jump to search
scientific article published on 03 October 2012
Language | Label | Description | Also known as |
---|---|---|---|
English | A novel 7 bp deletion in PRPF31 associated with autosomal dominant retinitis pigmentosa with incomplete penetrance in an Indian family |
scientific article published on 03 October 2012 |
Statements
A novel 7 bp deletion in PRPF31 associated with autosomal dominant retinitis pigmentosa with incomplete penetrance in an Indian family (English)
Seema Saini
Jai Rup Singh