The many faces of KIF7

Mutations in KIF7, the gene that encodes a component of the kinesin complex of anterograde intraflagellar transport in the cilia, have been reported to cause a range of phenotypes including hydrolethalis, acrocallosal syndrome and Joubert syndrome. In a cohort of patients with various neurogenetic p...

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Detalles Bibliográficos
Autores principales: Barakeh, Duna, Faqeih, Eissa, Anazi, Shams, S Al-Dosari, Mohammed, Softah, Ameen, Albadr, Fahad, Hassan, Hamdy, Alazami, Anas M, Alkuraya, Fowzan S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4785560/
https://www.ncbi.nlm.nih.gov/pubmed/27081521
http://dx.doi.org/10.1038/hgv.2015.6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4785560/
https://www.ncbi.nlm.nih.gov/pubmed/27081521
http://dx.doi.org/10.1038/hgv.2015.6

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