Adelaide Research & Scholarship
Browsing "Paediatrics publications" by Author Abbott, K.
Showing results 1 to 1 of 1
Preview | Issue Date | Title | Author(s) |
| 2015 | Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorder | Kumar, R.; Corbett, M.; Smith, N.; Jolly, L.; Tan, C.; Keating, D.; Duffield, M.; Utsumi, T.; Moriya, K.; Smith, K.; Hoischen, A.; Abbott, K.; Harbord, M.; Compton, A.; Woenig, J.; Arts, P.; Kwint, M.; Wieskamp, N.; Gijsen, S.; Veltman, J.; et al. |