Neuronal inclusions in the caudate nucleus of the brain in Huntington's disease, illustration. Inclusions are composed of mutated huntingtin protein, they are found in nuclei, axons and dendrites. Huntington's disease is a genetic neurodegenerative disease. It is autosomal dominant meaning that there is a 50% chance of offspring developing this disorder.
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Creative#:
TPG32656684
Source:
達志影像
Authorization Type:
RF
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須由TPG 完整授權
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N/A
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artworkbasalgangliabraincaudatenucleuscentralnervoussystemcerebralhemispherechromosomecorpusstriatumgenegeneticshealthhuntingtonschoreaillustrationmedicalmedicinemovementdisordernervoussystemneuronaldegenerationneuropathycoronalsectionhuntingtonsdiseaseautosomaldominantchromosome4httgenehuntingtinprotein3d3dimensionalneuronalinclusionneuronalinclusionnobodyno-one
33d4artworkautosomalbasalbraincaudatecentralcerebralchoreachromosomechromosomecoronalcorpusdegenerationdimensionaldiseasedisorderdominantgangliagenegenegeneticshealthhemispherehtthuntingtinhuntingtonshuntingtonsillustrationinclusioninclusionmedicalmedicinemovementnervousnervousneuronalneuronalneuronalneuropathyno-onenobodynucleusproteinsectionstriatumsystemsystem
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