Citations for
1CDHR1
Biallelic mutation of protocadherin-21 (PCDH21) causes retinal degeneration in humans.
Henderson RH, Li Z, Abd El Aziz MM, Mackay DS, Eljinini MA, Zeidan M, Moore AT, Bhattacharya SS, Webster AR.
Mol Vis 16:46-52. 2010
2CDHR1, CORD15, PROM1
Mutations in PCDH21 cause autosomal recessive cone-rod dystrophy.
Ostergaard E, Batbayli M, Duno M, Vilhelmsen K, Rosenberg T.
J Med Genet 47(10):665-9. Epub 2010 Aug 30. 2010
3CDHR1, PROM1
Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice.
Yang Z, Chen Y, Lillo C, Chien J, Yu Z, Michaelides M, Klein M, Howes KA, Li Y, Kaminoh Y, Chen H, Zhao C, Chen Y, Al-Sheikh YT, Karan G, Corbeil D, Escher P, Kamaya S, Li C, Johnson S, Frederick JM, Zhao Y, Wang C, Cameron DJ, Huttner WB, Schorderet DF, Munier FL, Moore AT, Birch DG, Baehr W, Hunt DM, Williams DS, Zhang K.
J Clin Invest 118(8):2908-16. 2008
4CDHR1
Protocadherin-21 (PCDH21), a candidate gene for human retinal dystrophies.
Bolz H, Ebermann I, Gal A.
Mol Vis 11:929-33. 2005
5CDHR1, KCNV2, LRTM1, SENP1
Profile of the genes expressed in the human peripheral retina, macula, and retinal pigment epithelium determined through serial analysis of gene expression (SAGE).
Sharon D, Blackshaw S, Cepko CL, Dryja TP.
Proc Natl Acad Sci U S A 99(1):315-20. 2002
6CDHR1
Identification of three novel non-classical cadherin genes through comprehensive analysis of large cDNAs.
Nakajima D, Nakayama M, Kikuno R, Hirosawa M, Nagase T, Ohara O.
Brain Res Mol Brain Res 94(1-2):85-95. 2001