Cite
APA Citation
Khateb, S., Zelinger, L., Mizrahi-Meissonnier, L., Ayuso, C., Koenekoop, R. K., Laxer, U., Gross, M., Banin, E., & Sharon, D. (2014). a homozygous nonsense CEP250 mutation combined with a heterozygous nonsense C2orf71 mutation is associated with atypical Usher syndrome. Journal of medical genetics, 51(7), 460–469. http://access.bl.uk/ark:/81055/vdc_100137784825.0x000048