Exclusion of atypical vitelliform macular dystrophy from 8q24.3 and from other known macular degenerative loci [5]

American Journal of Human Genetics

Volumn 61, Issue 1, 1997, Pages 239-241

  Sohocki, M M ^a   Sullivan, L S ^a   Mintz Hittner, H A ^a   Small, K ^a   Ferrell, R E ^a   Daiger, S P ^a  

^a UNIVERSITY OF TEXAS SCHOOL OF PUBLIC HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE AMINOTRANSFERASE;

AUTOSOMAL DOMINANT DISORDER; BLINDNESS; CHROMOSOME 16; CHROMOSOME 8Q; HUMAN; LETTER; PHENOTYPE; PRIORITY JOURNAL; RETINA MACULA VITELLIFORM DEGENERATION;

EID: 0030802607     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0002-9297(07)64299-2     Document Type: Letter

References (18)

1. C Dib S Faure C Fizames D Samson V Drouot A Vignal P Millasseau A comprehensive genetic map of the human genome based on 5,264 microsatellites Nature 380 1996 152 154
2. K Evans A Fryer C Inglehearn J Duvall-Young JL Whittaker CY Gregory R Butler Genetic linkage of cone-rod dystrophy to chromosome 19q and evidence for segregation distortion Nat Genet 6 1994 210 213
3. RE Ferrell H Mintz Hittner JH Antoszyk Linkage of atypical vitelliform macular dystrophy (VMD-1) to the soluble glutamate pyruvate transaminase (GPT1) locus Am J Hum Genet 35 1983 78 84
4. S Gerber J-M Rozet D Bonneau E Souied A Camuzat J-L Dufier P Amalric A gene for late-onset fundus flavimaculatus with macular dystrophy maps to chromosome 1p13 Am J Hum Genet 56 1995 396 399
5. C Graff K Forsman C Larsson S Nordstrom L Lind K Johanson O Sandgren Fine mapping of Best's macular dystrophy localizes the gene in close proximity to but distinct from the D11S480/ROM1 loci Genomics 24 1994 425 434
6. H Kremer A Pinckers B Van den Heim AF Deutman HH Ropers ECM Mariman Localization of the gene for dominant cystoid macular dystrophy on chromosome 7p Hum Mol Genet 3 1994 299 302
7. GM Lathrop JM Lalouel C Julier J Ott Strategies for multipoint linkage analysis in humans Proc Natl Acad Sci USA 81 1984 3443 3446
8. RJ Leach SS Banga K Ben-Othame S Chughtai R Clarke SP Daiger J Kolehmainen Report of the Third International Workshop on Human Chromosome 8 Mapping Cytogenet Cell Genet 75 1996 71 84
9. H Mintz-Hittner RE Ferrell RP Borda J Justice Jr Atypical vitelliform macular dystrophy in a 5-generation family Br J Ophthalmol 68 1984 199 207
10. KW Small M Syrquin L Mellen K Gehrs Mapping of autosomal dominant cone degeneration to chromosome 17p Am J Ophthalmol 121 1996 13 18
11. KW Small JL Weber A Roses F Lennon JM Vance MA Pericak-Vance North Carolina macular dystrophy is localized to 6q14-q16.2 Am J Hum Genet Suppl 51 1992 A34
12. MM Sohocki LS Sullivan WR Harrison EJ Sodergen FFB Elder G Weinstock S Tanase Human glutamate pyruvate transaminase (GPT): localization to 8q24.3, cDNA and genomic sequences, and polymorphic sites Genomics 40 1997 247 252
13. EM Stone BE Nichols AE Kimura TA Weingeist A Drack VC Sheffield Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6q Arch Ophthalmol 112 1994 765 772
14. BHF Weber G Vogt RC Pruett H Stohr U Felbor Mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) in patients with Sorsby's fundus dystrophy Nat Genet 8 1994 352 356
15. SG Welch Quantitative differences between the human red cell glutamate-pyruvate transaminase phenotypes Hum Hered 22 1972 190 197
16. SD Wijesuriya K Evans MR Jay C Davison BHF Weber AC Bird SS Bhattacharya Sorsby's fundus dystrophy in the British Isles: demonstration of a striking founder effect by microsatellite-generated haplotypes Genome Res 6 1996 92 101
17. LMM Wijnen P Meera Khan Assignment of GPT to human chromosome 16 Cytogenet Cell Genet 32 1982 327
18. K Zhang PP Bither R Parl LA Donoso JG Seidman CE Seidman A dominant Stargardt's macular dystrophy locus maps to chromosome 13q34 Arch Ophthalmol 112 1994 759 764