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An Iranian family with Alzheimer's disease caused by a novel APP mutation (Thr714Ala)
Pasalar, P., Najmabadi, H., Noorian, A. R., Moghimi, B., Jannati, A., Soltanzadeh, A., Krefft, T., Crook, R., Hardy, J.Volume:
58
Language:
english
Journal:
Neurology
DOI:
10.1212/WNL.58.10.1574
Date:
May, 2002
File:
PDF, 4.41 MB
english, 2002