reference/2697533

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startingPage	625
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bibliographicCitation	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. PMID: 25114083; PMCID: PMC4337967.
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date	2014-11-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC4337967 https://pubmed.ncbi.nlm.nih.gov/25114083 https://doi.org/10.3233/jad-141512
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	A Phenotype of Atypical Apraxia of Speech in a Family Carrying SQSTM1 Mutation
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