orient
发表于 2025-3-25 06:13:26
https://doi.org/10.1007/978-3-8350-9626-4ons and cognitive decline. The specific mutation responsible for HD is an expanded CAG repeat in exon 1 of the Huntington gene. This mutation can now be easily detected through genetic testing, allowing for confirmation of the genetic status in individuals at risk of developing HD, which occurs at a
Servile
发表于 2025-3-25 07:34:40
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抑制
发表于 2025-3-25 13:22:18
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hedonic
发表于 2025-3-25 19:00:19
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进入
发表于 2025-3-25 22:26:01
https://doi.org/10.1007/978-3-322-95093-2e only portion of the central nervous system that is optically accessible for high-resolution imaging. Over the last several decades there has been significant interest in leveraging the optical accessibility of the retina to understand, diagnose and monitor neurological diseases such as Huntington’
condone
发表于 2025-3-26 01:54:49
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myalgia
发表于 2025-3-26 06:11:05
Wolfgang H. C. Junge,Martina Jungegenesis of HD is progressive with a long premanifest phase in which subtle changes in the brain occur up to two decades before the onset of clinical symptoms. Early biomarkers reflecting the subtle changes in the HD brain for better understanding disease progression and evaluating treatment efficacy
maudtin
发表于 2025-3-26 08:51:39
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troponins
发表于 2025-3-26 13:05:44
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CONE
发表于 2025-3-26 20:31:51
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