Deficiency in Origin Licensing Proteins Impairs Cilia Formation: Implications for the Aetiology of Meier-Gorlin Syndrome

Mutations in ORC1, ORC4, ORC6, CDT1, and CDC6, which encode proteins required for DNA replication origin licensing, cause Meier-Gorlin syndrome (MGS), a disorder conferring microcephaly, primordial dwarfism, underdeveloped ears, and skeletal abnormalities. Mutations in ATR, which also functions duri...

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Detalles Bibliográficos
Autores principales: Stiff, Tom, Alagoz, Meryem, Alcantara, Diana, Outwin, Emily, Brunner, Han G., Bongers, Ernie M. H. F., O'Driscoll, Mark, Jeggo, Penny A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3597520/
https://www.ncbi.nlm.nih.gov/pubmed/23516378
http://dx.doi.org/10.1371/journal.pgen.1003360

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3597520/
https://www.ncbi.nlm.nih.gov/pubmed/23516378
http://dx.doi.org/10.1371/journal.pgen.1003360

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