Gene symbol: CYP1B1: Disease: Glaucoma, primary congenital

Human Genetics

Volumn 113, Issue 6, 2003, Pages 556-

  Chakrabarti, Subhabrata ^a   Komatireddy, Sreelatha ^a   Mandal, Anil Kumar ^a   Balasubramanian, Dorairajan ^a  

^a L V PRASAD EYE INSTITUTE   (India)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID SUBSTITUTION; BASE PAIRING; CODON; CONGENITAL GLAUCOMA; MISSENSE MUTATION; NONSENSE MUTATION; NOTE; NUCLEIC ACID BASE SUBSTITUTION; PRIMARY GLAUCOMA; PRIORITY JOURNAL; ARTICLE; GENETICS; GLAUCOMA; HUMAN; NOMENCLATURE; POINT MUTATION; NUCLEOTIDE SEQUENCE;

CYTOCHROME P 450 CYP1B1; CYTOCHROME P-450 CYP1B1; UNSPECIFIC MONOOXYGENASE; AMINO ACID; NUCLEOTIDE;

AMINO ACID SUBSTITUTION; ARYL HYDROCARBON HYDROXYLASES; GLAUCOMA; HUMANS; POINT MUTATION; TERMINOLOGY;

EID: 0242522114     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00439-003-1035-0     Document Type: Note

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