Genes associated with human glaucoma

Ophthalmology Clinics of North America

Volumn 18, Issue 3, 2005, Pages 335-343

  Wiggs, Janey L ^a  

^a MASSACHUSETTS EYE AND EAR INFIRMARY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME P450 1B1; MYOCILIN; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR PAX6; TRANSCRIPTION FACTOR PITX2;

CELL FUNCTION; CONGENITAL GLAUCOMA; DIAGNOSTIC TEST; GENE IDENTIFICATION; GENE LOCUS; GENE MUTATION; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GLAUCOMA; HUMAN; INTRAOCULAR PRESSURE; LOW TENSION GLAUCOMA; MICROPHTHALMIA; MISSENSE MUTATION; NONHUMAN; NUCLEOTIDE SEQUENCE; ONSET AGE; OPEN ANGLE GLAUCOMA; PATHOPHYSIOLOGY; PIGMENT DISORDER; PIGMENT DISPERSION SYNDROME; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; PSEUDOEXFOLIATION; RETINA GANGLION CELL; REVIEW;

GLAUCOMA, OPEN-ANGLE; HUMANS; INTRAOCULAR PRESSURE;

EID: 23044478011     PISSN: 08961549     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ohc.2005.05.003     Document Type: Review

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