Localization of the mouse nob (no b-wave) gene to the centromeric region of the X chromosome

Investigative Ophthalmology and Visual Science

Volumn 40, Issue 11, 1999, Pages 2748-2751

  Candille, Sophie I ^d   Pardue, Machelle T ^a,b   McCall, Maureen A ^d   Peachey, Neal S ^a,b   Gregg, Ronald G ^c  

^a HINES VA HOSPITAL   (United States)

^b LOYOLA UNIVERSITY CHICAGO   (United States)

^c UNIVERSITY OF LOUISVILLE   (United States)

^d NONE

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; ELECTRORETINOGRAPHY; GENE LOCATION; GENE MAPPING; GENOTYPE; MOUSE; NIGHT BLINDNESS; NONHUMAN; PATHOGENESIS; PEDIGREE; PHENOTYPE; PRIORITY JOURNAL; X CHROMOSOME;

ANIMALS; CENTROMERE; CHROMOSOME MAPPING; DISEASE MODELS, ANIMAL; ELECTRORETINOGRAPHY; FEMALE; GENOTYPE; LINKAGE (GENETICS); LOD SCORE; MALE; MICE; MICE, INBRED BALB C; MICE, INBRED C57BL; MICE, MUTANT STRAINS; NIGHT BLINDNESS; PEDIGREE; X CHROMOSOME;

EID: 0032833359     PISSN: 01460404     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (14)

1. Molday RS. Photoreceptor membrane proteins, phototransduction, and retinal degenerative diseases. The Friedenwald Lecture. Invest Ophthalmol Vis Sci. 1998;39:2491-2513.
2. Krill AE, Martin D. Photopic abnormalities in congenital stationary nightblindness. Invest Ophthalmol. 1971;10:625-636.
3. Dryja TP, Berson EL, Rao VR, Oprian DD. Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness. Nat Genet. 1993;4:280-283.
4. Dryja TP, Hahn LB, Reboul T, Arnaud B. Missense mutation in the gene encoding the a subunit of rod transducin in the Nougaret form of congenital stationary night blindness. Nat Genet. 1996;13:358-360.
5. Miyake Y, Yagasaki K, Horiguchi M, Kawase Y, Kanda T. Congenital stationary night blindness with negative electroretinogram. A new classification. Arch Ophthalmol. 1986;104:1013-1020.
6. Boycott KM, Pearce WG, Musarella MA, et al. Evidence for genetic heterogeneity in X-linked congenital stationary night blindness. Am J Hum Genet. 1998;62:865-875.
7. 1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness. Nat Genet. 1998;19:264-267.
8. Strom TM, Nyakatura G, Apfelstedt-Sylla E, et al. An L-type calcium channel gene mutated in incomplete X-linked congenital stationary night blindness. Nat Genet. 1998;19:260-263.
9. Pardue MT, McCall MA, LaVail MM, Gregg RG, Peachey NS. A naturally occurring mouse model of X-linked congenital stationary night blindness. Invest Ophthalmol Vis Sci. 1998;039:2443-2449.
10. Meindl A, Dry K, Herrmann K, et al. A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3). Nat Genet. 1996;13:35-42.
11. Yan D, Swain PK, Breuer D, et al. Biochemical characterization and subcellular localization of the mouse retinitis pigmentosa GTPase regulator (mRpgr). J Biol Chem. 1998;273:19656-19663.
12. Thiselton DL, Hampson RM, Nayudu M, et al. Mapping the RP2 locus for X-linked retinitis pigmentosa on proximal Xp: a genetically defined 5-cM critical region and exclusion of candidate genes by physical mapping. Genome Res. 1996;6:1093-1102.
13. Schwahn U, Lenzner S, Dong J, et al. Positional cloning of the gene for X-linked retinitis pigmentosa 2. Nat Genet. 1998;19: 327-332.
14. Seymour AB, Dash-Modi A, O'Connell JR, et al. Linkage analysis of X-linked cone-rod dystrophy: localization to Xp11.4 and definition of a locus distinct from RP2 and RP3. Am J Hum Genet. 1998;62:122-129.