Gene symbol: CYP1B1. Disease: Primary congenital glaucoma. Accession #Hd0515.

Human genetics

Volumn 118, Issue 6, 2006, Pages 775-

  Nirmaladevi, J ^a   Karthiyayini, T ^a   Kumaramanickavel, G ^a  

^a SANKARA NETHRALAYA   (India)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME P 450 CYP1B1; CYTOCHROME P-450 CYP1B1; UNCLASSIFIED DRUG; UNSPECIFIC MONOOXYGENASE;

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

ARYL HYDROCARBON HYDROXYLASES; BASE SEQUENCE; GENE DELETION; GLAUCOMA; HUMANS; AMINO ACID SUBSTITUTION; MUTATION, MISSENSE;

EID: 33847736671     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)