A Primary Microcephaly Protein Complex forms a ring around parental centrioles

Autosomal recessive primary microcephaly (MCPH) is characterised by a significant reduction in prenatal human brain growth, without alteration of cerebral architecture. The genetic aetiology of MCPH is bi-allelic mutations in genes coding for a subset of centrosomal proteins(1-10). While at least th...

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Detalles Bibliográficos
Autores principales: Sir, Joo-Hee, Barr, Alexis R., Nicholas, Adeline K., Carvalho, Ofelia P., Khurshid, Maryam, Sossick, Alex, Reichelt, Stefanie, D’Santos, Clive, Woods, C. Geoffrey, Gergely, Fanni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2011
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3299569/
https://www.ncbi.nlm.nih.gov/pubmed/21983783
http://dx.doi.org/10.1038/ng.971

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3299569/
https://www.ncbi.nlm.nih.gov/pubmed/21983783
http://dx.doi.org/10.1038/ng.971

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