The missense genetic polymorphisms of human CYP2A13: functional significance in carcinogen activation and identification of a null allelic variant.
Toxicol Sci
; 94(1): 38-45, 2006 Nov.
Article
in En
| MEDLINE
| ID: mdl-16917071
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Polymorphism, Genetic
/
Aryl Hydrocarbon Hydroxylases
/
Mutation, Missense
Type of study:
Diagnostic_studies
/
Prognostic_studies
Limits:
Animals
/
Humans
Language:
En
Journal:
Toxicol Sci
Journal subject:
TOXICOLOGIA
Year:
2006
Document type:
Article
Affiliation country:
United States