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