Can bioinformatics help trace the steps from gene mutation to disease?

Neurology

Volumn 55, Issue 3, 2000, Pages 331-333

  Graf, William D ^a,b  

^a UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

^b SEATTLE CHILDREN S RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; DNA; MESSENGER RNA; RNA;

ADRENOLEUKODYSTROPHY; AGYRIA; AMYOTROPHIC LATERAL SCLEROSIS; ATAXIA TELANGIECTASIA; BIOTECHNOLOGY; DNA SEQUENCE; EDITORIAL; GENE MUTATION; GENETIC MODEL; GENOME; HUMAN; NEUROFIBROMATOSIS; NEUROLOGIC DISEASE; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; THOMSEN DISEASE; WILSON DISEASE;

EID: 0033841849     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.55.3.331     Document Type: Editorial

References (11)

1. Mutation spectrum and predicted function of laforin in Lafora's progressive myoclonus epilepsy
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3. Basic local alignment search tool
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6. Biosequence exegesis
7. Keeping genome databases clean and up to date
8. Structural genomics: Beyond the Human Genome Project
9. Molecular classification of cancer: Class discovery and class prediction by gene expression monitoring
10. DNA microarrays in drug discovery and development
11. Do-it-yourself gene watching