Mutations in a Guanylate Cyclase GCY-35/GCY-36 Modify Bardet-Biedl Syndrome–Associated Phenotypes in Caenorhabditis elegans

Ciliopathies are pleiotropic and genetically heterogeneous disorders caused by defective development and function of the primary cilium. Bardet-Biedl syndrome (BBS) proteins localize to the base of cilia and undergo intraflagellar transport, and the loss of their functions leads to a multisystemic c...

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Detalles Bibliográficos
Autores principales: Mok, Calvin A., Healey, Michael P., Shekhar, Tanvi, Leroux, Michel R., Héon, Elise, Zhen, Mei
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/PMC3192831/
https://www.ncbi.nlm.nih.gov/pubmed/22022287
http://dx.doi.org/10.1371/journal.pgen.1002335

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3192831/
https://www.ncbi.nlm.nih.gov/pubmed/22022287
http://dx.doi.org/10.1371/journal.pgen.1002335

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