Clinical and genetic evidence for autosomal dominant North Carolina macular dystrophy in a German family

American Journal of Ophthalmology

Volumn 124, Issue 3, 1997, Pages 412-415

  Pauleikhoff, D ^a   Sauer, C G ^a   Muller, C R ^a   Radermacher, M ^a   Merz, A ^a   Weber, B H F ^a  

^a UNIVERSITY OF WÜRZBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ARTICLE; CHROMOSOME 6Q; CLINICAL ARTICLE; DRUSEN; FAMILY; FEMALE; GENE FREQUENCY; GENE MAPPING; GENETIC LINKAGE; GENOTYPE; GERMANY; HUMAN; MALE; OPHTHALMOSCOPY; PEDIGREE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RETINA MACULA DEGENERATION; SUBRETINAL NEOVASCULARIZATION;

EID: 0030848880     PISSN: 00029394     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9394(14)70842-6     Document Type: Article

References (4)

1. WH Lefler JAC Wadsworth JB Sidbury Hereditary macular degeneration and aminoaciduria Am J Ophthalmol 71 1971 224 230
2. KW Small JL Weber A Roses F Lennon JM Vance MA Pericak-Vance North Carolina macular dystrophy is assigned to chromosome 6 Genomics 13 1992 681 685
3. KW Small B Puech L Mullen S Yelchitis North Carolina macular dystrophy phenotype in France maps to the MCDR1 locus Mol Vis 3 1997 1 6
4. GM Lathrop JM Lalouel C Julier J Ott Multilocus linkage analysis in humans: detection of linkage and estimation of recombination Am J Hum Genet 37 1985 482 498