Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F

Canadian Journal of Ophthalmology

Volumn 35, Issue 4, 2000, Pages 204-213

  Boycott, Kym M ^a   Pearce, William G ^b   Bech Hansen, N Torben ^a  

^a UNIVERSITY OF CALGARY   (Canada)

^b UNIVERSITY OF ALBERTA   (Canada)

Author keywords

Incomplete congenital stationary night blindness; Mennonite; Myopia; Night blindness; Nystagmus; Visual acuity

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; CONGENITAL BLINDNESS; CONTROLLED STUDY; DARK ADAPTATION; DNA SEQUENCE; FEMALE; GENE EXPRESSION; GENE INSERTION; GENE MUTATION; GENETIC ANALYSIS; GENETIC VARIABILITY; HUMAN; MAJOR CLINICAL STUDY; MALE; MYOPIA; NIGHT VISION; NYSTAGMUS; OPHTHALMOSCOPY; PHENOTYPE; STRABISMUS; VISUAL ACUITY; X CHROMOSOMAL INHERITANCE;

EID: 0033744810     PISSN: 00084182     EISSN: 17153360     Source Type: Journal    
DOI: 10.1016/S0008-4182(00)80031-9     Document Type: Article

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