Novel Frem1-Related Mouse Phenotypes and Evidence of Genetic Interactions with Gata4 and Slit3

The FRAS1-related extracellular matrix 1 (FREM1) gene encodes an extracellular matrix protein that plays a critical role in the development of multiple organ systems. In humans, recessive mutations in FREM1 cause eye defects, congenital diaphragmatic hernia, renal anomalies and anorectal malformatio...

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Detalles Bibliográficos
Autores principales: Beck, Tyler F., Shchelochkov, Oleg A., Yu, Zhiyin, Kim, Bum Jun, Hernández-García, Andrés, Zaveri, Hitisha P., Bishop, Colin, Overbeek, Paul A., Stockton, David W., Justice, Monica J., Scott, Daryl 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/PMC3594180/
https://www.ncbi.nlm.nih.gov/pubmed/23536828
http://dx.doi.org/10.1371/journal.pone.0058830

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3594180/
https://www.ncbi.nlm.nih.gov/pubmed/23536828
http://dx.doi.org/10.1371/journal.pone.0058830

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