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Exome sequencing overrides formal genetics: ASPM mutations in a case study of apparent X-linked microcephalic intellectual deficit

Detalles Bibliográficos
Autores principales:	Ariani, F, Mari, F, Amitrano, S, Di Marco, C, Artuso, R, Scala, E, Meloni, I, Della Volpe, R, Rossi, A, Bokhoven, H, Renieri, A
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Blackwell Publishing Ltd 2013
Materias:	Letters to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648977/ https://www.ncbi.nlm.nih.gov/pubmed/22823409 http://dx.doi.org/10.1111/j.1399-0004.2012.01901.x

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