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JAD-2011-102124
JAD-2011-102124
http://dx.doi.org/10.3233/JAD-2011-102124
A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia.
P356
Q30402493-96424654-07E0-4541-A046-B9987790AF77
P356
JAD-2011-102124
http://dx.doi.org/10.3233/JAD-2011-102124