Linkage and mutational analysis of familial Alzheimer disease kindreds for the APP gene region

A large number of familial Alzheimer disease (FAD) kindreds were examined to determine whether mutations in the amyloid precursor protein (APP) gene could be responsible for the disease. Previous studies have identified three mutations at APP codon 717 which are pathogenic for Alzheimer disease (AD)...

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محفوظ في:
التفاصيل البيبلوغرافية
المؤلفون الرئيسيون: Kamino, Kouzin, Orr, Harry T., Payami, Haydeh, Wijsman, Ellen M., Alonso, Ma. Elisa, Pulst, Stefan M., Anderson, Leojean, O'dahl, Sheldon, Nemens, Ellen, White, June A., Sadovnick, Adele D., Ball, Melvyn J., Kaye, Jeffery, Warren, Andrew, McInnis, Melvin, Antonarakis, Stylianos E., Korenberg, Julie R., Sharma, Vikram, Kukull, Walter, Larson, Eric, Heston, Leonard L., Martin, George M., Bird, Thomas D., Schellenberg, Gerard D.
التنسيق: Artigo
اللغة:Inglês
منشور في: 1992
الموضوعات:
Original Articles
الوصول للمادة أونلاين:https://ncbi.nlm.nih.gov/pmc/articles/PMC1682859/
https://ncbi.nlm.nih.gov/pubmed/1415269
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