Molecular genesis of Huntington's disease, illustration. Expansion of the CAG trinucleotide sequence in the htt gene causes production of mutated Huntingtin protein leading to neurodegeneration, atrophy of brain basal ganglia, involuntary movements and dementia.
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TPG32758427
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達志影像
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RF
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33d4acidanatomicalanatomyartworkautosomalbasalbraincaudatecentralcerebralchoreachoreachoreachoreiformchromosomechromosomecoronalcorpusdegenerationdegenerationdegradationdeoxyribonucleicdimensionaldiseasediseasedisorderdnadominantgangliagenegenegeneticshealthhemispherehtthuntingtinhuntingtonhuntingtonhuntingtonshuntingtonsillustrationinvoluntarylentiformmalemanmedicalmedicinemhhtmolecularmoleculemovementmovementsmovementsmutantmutatednervousnervousneuronneuronalneuropathyno-onenobodynucleusnucleusproteinputamensectionstriatumstructuresystemsystem
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