Abrams, A. ., Hufnagel, R. ., Rebelo, A. ., Zanna, C. ., Patel, N. ., Gonzalez, M. ., … Dallman, J. . (2015). Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder. Nature Genetics, 47(8), 926-32. https://doi.org/10.1038/ng.3354
CA Prows
First name:
CA
Last name:
Prows
Hufnagel, R. ., Arno, G. ., Hein, N. ., Hersheson, J. ., Prasad, M. ., Anderson, Y. ., … Ahmed, Z. . (2015). Neuropathy target esterase impairments cause Oliver-McFarlane and Laurence-Moon syndromes. Journal of Medical Genetics, 52(2), 85-94. https://doi.org/10.1136/jmedgenet-2014-102856