Phenotypic heterogeneity of CYP1B1: Mutations in a patient with Peters' anomaly [2]

Journal of Medical Genetics

Volumn 38, Issue 5, 2001, Pages 324-326

  Vincent, Andrea ^a,b,c   Billingsley, Gail ^b,c   Priston, Megan ^c   Williams Lyn, Donna ^c   Sutherland, Joanne ^a   Glaser, Tom ^d   Oliver, Edward ^d   Walter, Michael A ^e   Heathcote, Godfrey ^f   Levin, Alex ^a,b   Héon, Elise ^a,b,c  

^a HOSPITAL FOR SICK CHILDREN   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

^c TORONTO WESTERN HOSPITAL   (Canada)

^d UNIVERSITY OF MICHIGAN HEALTH SYSTEM   (United States)

^e UNIVERSITY OF ALBERTA   (Canada)

^f UNIVERSITY OF WESTERN ONTARIO   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME P450 1B1;

CASE REPORT; CONGENITAL GLAUCOMA; GENE MUTATION; GENETIC HETEROGENEITY; HUMAN; LETTER; MALE; PETERS ANOMALY; PRESCHOOL CHILD; PRIORITY JOURNAL; TRABECULECTOMY;

AMINO ACID SEQUENCE; ARYL HYDROCARBON HYDROXYLASES; BASE SEQUENCE; CANADA; CHILD; CHILD, PRESCHOOL; CYTOCHROME P-450 ENZYME SYSTEM; GLAUCOMA; HUMANS; INDIANS, NORTH AMERICAN; INFANT; INFANT, NEWBORN; MALE; MUTATION; PHENOTYPE;

EID: 0035039383     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

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