Novel locus for autosomal recessive cone-rod dystrophy CORD8 mapping to chromosome 1q12-Q24

Investigative Ophthalmology and Visual Science

Volumn 41, Issue 12, 2000, Pages 3709-3712

  Khaliq, S ^a   Hameed, A ^a   Ismail, M ^a   Anwar, K ^a   Leroy, B P ^a   Mehdi, S Q ^a   Payne, A M ^a   Bhattacharya, S S ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 1Q; CHROMOSOME MAP; GENE DELETION; GENETIC ANALYSIS; HUMAN; HUMAN TISSUE; OPHTHALMOSCOPY; PHOTORECEPTOR CELL; PRIORITY JOURNAL; RETINA BLOOD VESSEL; RETINA CONE; RETINA DYSTROPHY; RETINA MACULA DEGENERATION; RETINA ROD;

ADOLESCENT; CHILD; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 1; COLOR VISION DEFECTS; CONSANGUINITY; DNA; FEMALE; HUMANS; LACRIMAL APPARATUS DISEASES; LINKAGE (GENETICS); MALE; MICROSATELLITE REPEATS; NIGHT BLINDNESS; PEDIGREE; PHOTOPHOBIA; PHOTORECEPTORS, VERTEBRATE; POTASSIUM CHANNELS; POTASSIUM CHANNELS, INWARDLY RECTIFYING; RECEPTORS, RETINOIC ACID; RETINAL DEGENERATION; TRANSDUCIN;

EID: 0033753625     PISSN: 01460404     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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