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Volumn 87, Issue 1, 2003, Pages 2-3
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The OPA1 gene and optic neuropathy
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Author keywords
[No Author keywords available]
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Indexed keywords
MYOCILIN;
AUTOSOMAL DOMINANT DISORDER;
CELL DEGENERATION;
CHROMOSOME 1Q;
CHROMOSOME 3Q;
DNA POLYMORPHISM;
FAMILY HISTORY;
GENE EXPRESSION;
GENE INTERACTION;
GENE MUTATION;
GENE SEQUENCE;
GENETIC LINKAGE;
GENETIC VARIABILITY;
GLAUCOMA;
HUMAN;
INTRAOCULAR PRESSURE;
MULTIGENE FAMILY;
NERVE CELL NECROSIS;
OPEN ANGLE GLAUCOMA;
OPTIC NERVE;
OPTIC NERVE ATROPHY;
OPTIC NERVE DISEASE;
PALLOR;
PEDIGREE;
PREVALENCE;
PRIORITY JOURNAL;
RETINA GANGLION CELL;
REVIEW;
SEQUENCE ANALYSIS;
VISION;
VISUAL FIELD;
VISUAL IMPAIRMENT;
CELL DEATH;
CHILD;
GLAUCOMA;
GTP PHOSPHOHYDROLASES;
HUMANS;
OPTIC ATROPHY, AUTOSOMAL DOMINANT;
OPTIC NERVE;
PHENOTYPE;
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EID: 0037230231
PISSN: 00071161
EISSN: None
Source Type: Journal
DOI: 10.1136/bjo.87.1.2 Document Type: Review |
Times cited : (7)
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References (12)
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