Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotype

✍ Scribed by Filges, I.; Nosova, E.; Bruder, E.; Tercanli, S.; Townsend, K.; Gibson, W.T.; Röthlisberger, B.; Heinimann, K.; Hall, J.G.; Gregory-Evans, C.Y.; Wasserman, W.W.; Miny, P.; Friedman, J.M.

• Book ID: 121715869
• Publisher: John Wiley and Sons
• Year: 2013
• Tongue: English
• Weight: 736 KB
• Volume: 86
• Category: Article
• ISSN: 0009-9163
• DOI: 10.1111/cge.12301