Author:
Comitato Antonella,Spampanato Carmine,Chakarova Christina,Sanges Daniela,Bhattacharya Shomi S.,Marigo Valeria
Publisher
Oxford University Press (OUP)
Subject
Genetics (clinical),Genetics,Molecular Biology,General Medicine
Reference25 articles.
1. A human homolog of yeast pre-mRNA splicing gene, PRP31, underlies autosomal dominant retinitis pigmentosa on chromosome 19q13.4 (RP11);Vithana;Mol. Cell,2001
2. Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13);McKie;Hum. Mol. Genet.,2001
3. PAP-1, the mutated gene underlying the RP9 form of dominant retinitis pigmentosa, is a splicing factor;Maita;Exp. Cell Res,2004
4. Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa;Chakarova;Hum. Mol. Genet.,2002
5. A ninth locus (RP18) for autosomal dominant retinitis pigmentosa maps in the pericentromeric region of chromosome 1;Xu;Hum. Mol. Genet.,1996
Cited by
39 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献