oXXLcSvznKG7M7/lqLjoImrc534I19sG0nnW1IPahEox//dltru43Vaxd+Su5x9em7TH42adOXJFyeGC7mvhuW/27fjGvquuk2cc
6hGIEHWCLyROExALjpGXoAL0TgrAXS4BUZxLulr///Lu/EpiCa5D3429cQBGJRw/EMKHjChNSYxJnp1YV4Ps2kYaU0cc+/Y
7+Cc/IgcePNr64dTQWV3oLH8NTxOWYwHyaraQQMf8yQe+w4yF27D4CUjaCtQ671acsfxw1tMyfeHz1**5aL8N5dPbfVAU37
4yFZ7CNk65+cC3HqQ//x/ZE2NpE8bCtgfCLRuhYP2i4Pq906euRQ+uiy6PcGnZaZcjU8rKBkCKePTT/5Jrs9I1IAfyrz8+/HsS
很可能AD的可能性。只建议应用于科研或临床试验家族型类似症状的家族史,特别是经尸检诊断为AD易感基因(APP、PSEN1、PSEN2)证据增加AD病变可能性。此类型中APOE-4等位基因并无足够的特异
oXXLcSvznKG7M7/lqLjoImrc534I19sG0nnW1IPahEox//dltru43Vaxd+Su5x9em7TH42adOXJFyeGC7mvhuW/27fjGvquuk2cc