Conclusive evidence for a distinct congenital stationary night blindness locus in Xp21.1

Journal of Medical Genetics

Volumn 33, Issue 10, 1996, Pages 869-872

  Bergen, Arthur A B ^a   Ten Brink, J B ^a   Riemslag, F ^a,b   Schuurman, E J M ^a   Meire, F ^c   Tijmes, N ^a   De Jong, P T V M ^a,d  

^a NETHERLANDS INSTITUTE FOR NEUROSCIENCE   (Netherlands)

^b ACADEMIC MEDICAL CENTER   (Netherlands)

^c GHENT UNIVERSITY   (Belgium)

^d ERASMUS UNIVERSITY ROTTERDAM   (Netherlands)

Author keywords

Congenital stationary night blindness; Genetic mapping; Linkage analysis; X chromosome

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHROMOSOME XP; CLINICAL ARTICLE; CONTROLLED STUDY; GENE LOCUS; HUMAN; HUMAN CELL; MALE; NIGHT BLINDNESS; NIGHT VISION; PRIORITY JOURNAL; RETINA DISEASE; RETINITIS PIGMENTOSA; VISUAL ACUITY; X CHROMOSOME LINKAGE;

EID: 0029856584     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.33.10.869     Document Type: Article

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