A human laterality disorder associated with a homozygous WDR16 deletion

The laterality in the embryo is determined by left-right asymmetric gene expression driven by the flow of extraembryonic fluid, which is maintained by the rotary movement of monocilia on the nodal cells. Defects manifest by abnormal formation and arrangement of visceral organs. The genetic etiology...

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Detalles Bibliográficos
Autores principales: Ta-Shma, Asaf, Perles, Zeev, Yaacov, Barak, Werner, Marion, Frumkin, Ayala, Rein, Azaria JJT, Elpeleg, Orly
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Short Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4538206/
https://www.ncbi.nlm.nih.gov/pubmed/25469542
http://dx.doi.org/10.1038/ejhg.2014.265

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4538206/
https://www.ncbi.nlm.nih.gov/pubmed/25469542
http://dx.doi.org/10.1038/ejhg.2014.265

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