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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Bibliografiska uppgifter
Huvudupphovsmän: 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
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2011
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Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC3299569/
https://ncbi.nlm.nih.gov/pubmed/21983783
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.971
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