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

https://arctichealth.org/en/permalink/ahliterature194362
Source
J Med Genet. 2001 May;38(5):324-6
Publication Type
Article
Date
May-2001
More detail
Author
A. Vincent
G. Billingsley
M. Priston
D. Williams-Lyn
J. Sutherland
T. Glaser
E. Oliver
M A Walter
G. Heathcote
A. Levin
E. Héon
Source
J Med Genet. 2001 May;38(5):324-6
Date
May-2001
Language
English
Publication Type
Article
Keywords
Amino Acid Sequence
Aryl Hydrocarbon Hydroxylases
Base Sequence
Canada - ethnology
Child
Child, Preschool
Cytochrome P-450 Enzyme System - genetics
Glaucoma - congenital - enzymology - genetics - pathology
Humans
Indians, North American - genetics
Infant
Infant, Newborn
Male
Mutation - genetics
Phenotype
PubMed ID
11403040 View in PubMed
Less detail