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Models that express N-terminal fragments of HD exon 1 shows a rapid development of disease phenotype accompanied by motor deficits and weight loss seen in HD patients, whereas those models that contain the full-length murine Hdh gene demonstrate a lengthy disease course with attenuated motor defects and albeit specific neurodegeneration signs

What delivery route

[Benign symmetric Launois-Bensaude type III lipomatosis and Bureau-Barriere syndrome] [PubMed: 1874620] 256

Nutritional status of Iranian women with rheumatoid arthritis: An assessment of dietary intake and disease activity

The test looked at mental speed and flexibility