Molecular genetics of human blue cone monochromacy

Science

Volumn 245, Issue 4920, 1989, Pages 831-838

  Nathans, Jeremy ^a   Davenport, Carol M ^a   Maumenee, Irene H ^a   Lewis, Richard Alan ^b   Hejtmancik, J Fielding ^c   Litt, Michael ^d   Lovrien, Everett ^d   Weleber, Richard ^d   Bachynski, Brian ^e   Zwas, Fred ^f   Klingaman, Roger ^g   Fishman, Gerald ^h  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b CULLEN EYE INSTITUTE   (United States)

^c BAYLOR COLLEGE OF MEDICINE   (United States)

^d OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^e HENRY FORD HOSPITAL   (United States)

^f WAYNE STATE UNIVERSITY   (United States)

^g SOUTHERN COLLEGE OF OPTOMETRY   (United States)

^h UNIVERSITY OF ILLINOIS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

VISUAL PIGMENT;

COLOR BLINDNESS; HEREDITY; HUMAN; POINT MUTATION; PRIORITY JOURNAL;

ADOLESCENT; ADULT; BASE SEQUENCE; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; COLOR VISION DEFECTS; DNA; FEMALE; HUMAN; MALE; MOLECULAR SEQUENCE DATA; MUTATION; NUCLEIC ACID HYBRIDIZATION; RETINAL PIGMENTS; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.; THALASSEMIA; X CHROMOSOME;

EID: 0024449541     PISSN: 00368075     EISSN: None     Source Type: Journal    
DOI: 10.1126/science.2788922     Document Type: Article

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