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The top documents tagged [cag repeats]
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CNS NOTES
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Dementia
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© 2009 NHS National Genetics Education and Development CentreGenetics and Genomics for Healthcare Huntington Disease An overview
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Ataxin-3 Expression and HSR
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Huntington Disease (HD) This presentation includes: Clinical classification and features. Structure and molecular basis of the HD gene. Clinical photographs
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Dominant neurodegenerative disease Polyglutamine repeat expansions (CAG, codon, Q) in exon 1 of huntingtin gene (htt). Usually >35 CAG repeats
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OGMS Applied OGMS is the Ontology for General Medical Science, which provides definitions for all the terms (such as ‘disorder’, ‘symptom’, and so forth)
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Structural and Functional Analysis
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Huntington’s Disease Leon S. Dure, MD The University of Alabama at Birmingham
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ZEESHAN GAUHAR PhD SCHOLOR-BIOTECHNOLOGY 14-ARID-4978
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Genetics and Populations Chapter 14. Central Points Genetic conditions can be very common in a specific community Huntington disease affects large
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EUKARYOTIC GENE EXPRESSION. DNA PACKING Histones Nucleosomes (1 st ) 30nm fibers (2 nd ) Looped domains (3 rd ) Heterochromatin – not transcribed, metaphase
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