A phenotype of atypical apraxia of speech in a family carrying SQSTM1 mutation
携带SQSTM1突变的家族中出现非典型言语失用症的表型
期刊:Journal of Alzheimers Disease
影响因子:3.1
doi:10.3233/JAD-141512
Boutoleau-Bretonnière, Claire; Camuzat, Agnès; Le Ber, Isabelle; Bouya-Ahmed, Kawtar; Guerreiro, Rita; Deruet, Anne-Laure; Evrard, Christelle; Bras, José; Lamy, Estelle; Auffray-Calvier, Elisabeth; Pallardy, Amandine; Hardy, John; Brice, Alexis; Derkinderen, Pascal; Vercelletto, Martine