ISDN2014_0322: REMOVED: Identification of novel genetic causes of Rett syndrome‐like phenotypes by whole exome sequencing

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Lopes F, Barbosa M, Temudo T, de Sá J, Dias AI, Oliveira G, Cabral P, Calado E, Cruz IF, Soares G, Vieira JP, Venâncio MM, Oliveira R, Jonasson I, Ameur A, Pinto D, Ulf Gyllensten , Maciel P

Intl J of Devlp Neuroscience 47 (Part_A) 99-99 [2015-12-00; online 2015-11-05]

DOI 10.1016/j.ijdevneu.2015.04.269

Crossref 10.1016/j.ijdevneu.2015.04.269