Authors:
Sohocki, MM
Daiger, SP
Bowne, SJ
Rodriguez, JA
Northrup, H
Heckenlively, JR
Birch, DG
Mintz-Hittner, H
Ruiz, RS
Lewis, RA
Saperstein, DA
Sullivan, LS
Citation: Mm. Sohocki et al., Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies, HUM MUTAT, 17(1), 2001, pp. 42-51
Authors:
Bowne, SJ
Sullivan, LS
Ding, L
Traer, E
Prescott, SM
Birch, DG
Kennan, A
Humphries, P
Daiger, SP
Citation: Sj. Bowne et al., Evaluation of human diacylglycerol kinase, DGKI, a homolog of Drosophila rdgA, in inherited retinopathy mapping to 7q, MOL VIS, 6(2), 2000, pp. 6-9
Authors:
Sohocki, MM
Bowne, SJ
Sullivan, LS
Blackshaw, S
Cepko, CL
Payne, AM
Bhattacharya, SS
Khaliq, S
Mehdi, SQ
Birch, DG
Harrison, WR
Elder, FFB
Heckenlively, JR
Daiger, SP
Citation: Mm. Sohocki et al., Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenitalamaurosis, NAT GENET, 24(1), 2000, pp. 79-83
Authors:
Sullivan, LS
Heckenlively, JR
Bowne, SJ
Zuo, J
Hide, WA
Gal, A
Denton, M
Inglehearn, CF
Blanton, SH
Daiger, SP
Citation: Ls. Sullivan et al., Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosa, NAT GENET, 22(3), 1999, pp. 255-259
Authors:
Bowne, SJ
Daiger, SP
Hims, MM
Sohocki, MM
Malone, KA
McKie, AB
Heckenlively, JR
Birch, DG
Inglehearn, CF
Bhattacharya, SS
Bird, A
Sullivan, LS
Citation: Sj. Bowne et al., Mutations in the RP1 gene causing autosomal dominant retinitis pigmentosa, HUM MOL GEN, 8(11), 1999, pp. 2121-2128