Carpenter Syndrome: Extended RAB23 Mutation Spectrum and Analysis of Nonsense-mediated mRNA Decay

Carpenter syndrome, a rare autosomal recessive disorder characterized by a combination of craniosynostosis, polysyndactyly, obesity, and other congenital malformations, is caused by mutations in RAB23, encoding a member of the Rab-family of small GTPases. In 15 out of 16 families previously reported...

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Detalles Bibliográficos
Autores principales: Jenkins, Dagan, Baynam, Gareth, De Catte, Luc, Elcioglu, Nursel, Gabbett, Michael T, Hudgins, Louanne, Hurst, Jane A, Jehee, Fernanda Sarquis, Oley, Christine, Wilkie, Andrew O M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Subscription Services, Inc., A Wiley Company 2011
Materias:
Mutations in Brief
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3429868/
https://www.ncbi.nlm.nih.gov/pubmed/21412941
http://dx.doi.org/10.1002/humu.21457

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3429868/
https://www.ncbi.nlm.nih.gov/pubmed/21412941
http://dx.doi.org/10.1002/humu.21457

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