Probable Novel APP Met671Leu Mutation in a Chinese Han Family with Early-Onset Alzheimer’s Disease
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s12017-023-08770-1.pdf
Reference26 articles.
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3. Bagyinszky, E., Kang, M. J., Van Giau, V., Shim, K., Pyun, J. M., Suh, J., An, S. S. A., & Kim, S. (2019). Novel amyloid precursor protein mutation, Val669Leu (“Seoul APP”), in a Korean patient with early-onset Alzheimer’s disease. Neurobiology of Aging, 84(231), 236. https://doi.org/10.1016/j.neurobiolaging.2019.08.026
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