Identification of a Novel ZIC3 Isoform and Mutation Screening in Patients with Heterotaxy and Congenital Heart Disease

Patients with heterotaxy have characteristic cardiovascular malformations, abnormal arrangement of their visceral organs, and midline patterning defects that result from abnormal left-right patterning during embryogenesis. Loss of function of the transcription factor ZIC3 causes X-linked heterotaxy...

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Detalles Bibliográficos
Autores principales: Bedard, James E. J., Haaning, Allison M., Ware, Stephanie M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3157443/
https://www.ncbi.nlm.nih.gov/pubmed/21858219
http://dx.doi.org/10.1371/journal.pone.0023755

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3157443/
https://www.ncbi.nlm.nih.gov/pubmed/21858219
http://dx.doi.org/10.1371/journal.pone.0023755

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