Molecular and Cellular Basis of Autosomal Recessive Primary Microcephaly

Autosomal recessive primary microcephaly (MCPH) is a rare hereditary neurodevelopmental disorder characterized by a marked reduction in brain size and intellectual disability. MCPH is genetically heterogeneous and can exhibit additional clinical features that overlap with related disorders including...

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Detalles Bibliográficos
Autores principales: Barbelanne, Marine, Tsang, William Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4274849/
https://www.ncbi.nlm.nih.gov/pubmed/25548773
http://dx.doi.org/10.1155/2014/547986

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4274849/
https://www.ncbi.nlm.nih.gov/pubmed/25548773
http://dx.doi.org/10.1155/2014/547986

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