Gene symbol: CYP1B1. Disease: Glaucoma, primary congenital. Accession #Hd0513.

Human genetics

Volumn 118, Issue 6, 2006, Pages 775-

  Brinkmann, J F ^a   Ottenheim, C P ^a   Zegers, R H ^a   de Jong, P T ^a   Bergen, A A ^a  

^a NETHERLANDS INSTITUTE FOR NEUROSCIENCE   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

CYP1B1 PROTEIN, HUMAN; CYTOCHROME P450; UNCLASSIFIED DRUG; CYTOCHROME P 450 CYP1B1; CYTOCHROME P-450 CYP1B1; UNSPECIFIC MONOOXYGENASE;

ARTICLE; GENE DELETION; GENETICS; GLAUCOMA; HUMAN; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; AMINO ACID SUBSTITUTION; MISSENSE MUTATION;

BASE SEQUENCE; CYTOCHROME P-450 ENZYME SYSTEM; GENE DELETION; GLAUCOMA; HUMANS; MOLECULAR SEQUENCE DATA; AMINO ACID SUBSTITUTION; ARYL HYDROCARBON HYDROXYLASES; MUTATION, MISSENSE;

EID: 33847742185     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)