Medical genetics: advances in brief: Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci
AUTOR(ES)
Barber, John C K
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1016669Documentos Relacionados
- Defective subunit assembly underlies a digenic form of retinitis pigmentosa linked to mutations in peripherin/rds and rom-1
- Medical genetics: advances in brief: Medical genetics: advances in brief
- Medical genetics: advances in brief: Medical genetics: advances in brief
- Medical genetics: advances in brief: Medical genetics: advances in brief
- Medical genetics: advances in brief: Contribution of BRCA1 mutations to ovarian cancer