Assessment of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene localised to 6q13-q15 in autosomal dominant Stargardt-like disease (ADSTGD), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1)

Journal of Medical Genetics

Volumn 35, Issue 8, 1998, Pages 641-645

  Gehrig, Andrea ^a   Feibor, Ute ^a   Kelsell, Rosemary E ^b   Hunt, David M ^b   Maumenee, Irene H ^c   Weber, Bernhard H F ^a  

^a UNIVERSITY OF WÜRZBURG   (Germany)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

^c JOHNS HOPKINS UNIVERSITY   (United States)

Author keywords

Interphotoreceptor matrix proteoglycan 1; MCDR1; PBCRA; Stargardt like macular dystrophy

Indexed keywords

PROTEOGLYCAN;

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 13Q; CHROMOSOME 6Q; EXON; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE AMPLIFICATION; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENETIC LINKAGE; HUMAN; MAJOR CLINICAL STUDY; MALE; PHOTORECEPTOR CELL; PRIORITY JOURNAL; RETINA MACULA DEGENERATION; RETINOPATHY;

EID: 0031874062     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.35.8.641     Document Type: Article

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