Phenotypic heterogeneity of CYP1B1: mutations in a       patient with Peters' anomaly.

Vincent, A; Billingsley, G; Priston, M; Williams-Lyn, D; Sutherland, J; Glaser, T; Oliver, E; Walter, M A; Heathcote, G; Levin, A; Héon, E

Phenotypic heterogeneity of CYP1B1: mutations in a patient with Peters' anomaly.

Vincent, A; Billingsley, G; Priston, M; Williams-Lyn, D; Sutherland, J; Glaser, T; Oliver, E; Walter, M A; Heathcote, G; Levin, A; Héon, E.

J Med Genet ; 38(5): 324-6, 2001 May.

Article in En | MEDLINE | ID: mdl-11403040

Subject(s)

Aryl Hydrocarbon Hydroxylases; Cytochrome P-450 Enzyme System/genetics; Glaucoma/congenital; Glaucoma/genetics; Mutation/genetics; Amino Acid Sequence; Base Sequence; Canada/ethnology; Child; Child, Preschool; Cytochrome P-450 CYP1B1; Glaucoma/enzymology; Glaucoma/pathology; Humans; Indians, North American/genetics; Infant; Infant, Newborn; Male; Phenotype

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Aryl Hydrocarbon Hydroxylases / Glaucoma / Cytochrome P-450 Enzyme System / Mutation Limits: Child / Child, preschool / Humans / Infant / Male / Newborn Country/Region as subject: America do norte Language: En Journal: J Med Genet Year: 2001 Document type: Article Country of publication: United kingdom

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