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HTT gene CAG triplet repeat expansions in Huntington's disease (HD)... | Download Scientific Diagram
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CAG Repeats in the androgen receptor gene is associated with oligozoospermia and teratozoospermia in infertile men in Jordan - Al Zoubi - 2020 - Andrologia - Wiley Online Library
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The genetic 'gray area' of Huntington's disease: what does it all mean? - HDBuzz - Huntington's disease research news.
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The CAG-polyglutamine repeat diseases: a clinical, molecular, genetic, and pathophysiologic nosology. | Semantic Scholar
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A Worldwide Study of the Huntington's Disease Mutation: The Sensitivity and Specificity of Measuring CAG Repeats | NEJM
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Diagnostics | Free Full-Text | The Effect of CAG Repeats within the Non-Pathological Range in the HTT Gene on Cognitive Functions in Patients with Subjective Cognitive Decline and Mild Cognitive Impairment
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The Genetic Defect Causing Huntington's Disease: Repeated in Other Contexts? | Molecular Medicine | Full Text
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Frontiers | CAG Repeats Within the Non-pathological Range in the HTT Gene Influence Personality Traits in Patients With Subjective Cognitive Decline: A 13-Year Follow-Up Study
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PacBio on Twitter: "#DYK: Repeat expansions are mutations that result in repeating sequence that may extend to 1,000s of bases? The trinucleotide repeat expansion in Huntington's disease consists of 100s of C-A-G
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Ectopically Expressed CAG Repeats Cause Intranuclear Inclusions and a Progressive Late Onset Neurological Phenotype in the Mouse: Cell
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Transcription-Induced CAG Repeat Contraction in Human Cells Is Mediated in Part by Transcription-Coupled Nucleotide Excision Repair | Molecular and Cellular Biology
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Positive association of the androgen receptor CAG repeat length polymorphism with the risk of prostate cancer
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