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Unilateral transplantation of human primary fetal tissue in four patients with Huntington's disease: NEST-UK safety report ISRCTN no 36485475

Objectives: Huntington's disease (HD) is an inherited autosomal dominant condition in which there is a CAG repeat expansion in the huntingtin gene of 36 or more. Patients display progressive motor, cognitive, and behavioural deterioration associated with progressive cell loss and atrophy in the...

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書誌詳細
主要な著者: Rosser, A, Barker, R, Harrower, T, Watts, C, Farrington, M, Ho, A, Burnstein, R, Menon, D, Gillard, J, Pickard, J, Dunnett, S
フォーマット: Artigo
言語:Inglês
出版事項: BMJ Group 2002
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC1757375/
https://ncbi.nlm.nih.gov/pubmed/12438470
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp.73.6.678
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