Boutoleau-Bretonnière C, Camuzat A, Le Ber I, Bouya-Ahmed K, Guerreiro R, Deruet AL, Evrard C, Bras J, Lamy E, Auffray-Calvier E, Pallardy A, Hardy J, Brice A, Derkinderen P, Vercelletto M. A phenotype of atypical apraxia of speech in a family carrying SQSTM1 mutation. J Alzheimers Dis. 2015;43(2):625-30. PubMed.
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