B

Bennett, C.L., Lawson, V.H., Brickell, K.L., Isaacs, K., Seltzer, W., Lipe, H.P., Weiss, M.D., Carter, G.T., Flanigan, K.M., Chance, P.F., and Bird, T.D. (2008) Late-onset hereditary axonal neuropathies. Neurology, 71 (1). pp. 14-20.

D

de Jong, Danielle (2005) Characterisation of homologs of nervous system patterning genes in the staghorn coral, Acropora millepora (Cnidaria; Anthozoa; Scleractinia). PhD thesis, James Cook University.

Delatycki, M.B., Paris, D., Gardner, R.J.M., Forshaw, K., Nicholson, G.A., Nassif, N., Williamson, R., and Forrest, S.M. (1998) Sperm DNA analysis in a Friedreich ataxia premutation carrier suggests both meiotic and mitotic expansion in the FRDA gene. Journal of Medical Genetics, 35. pp. 713-716.

F

Forrest, S.M., Delatycki, M., Paris, D., Gardner, R.J.M., Forshaw, K., Nicholson, G., Nassis, N., Williamson, R., and UNSPECIFIED (1997) The Friedreich's ataxia mutation may originate from a premutation and shows size reduction when transmitted from parent to affected child. American Journal of Human Genetics, 61 (Suppl). 1799. A308-A308.

G

Gottschalk, Michael G., Sarnyai, Zoltan, Guest, Paul C., Harris, Laura W., and Bahn, Sabine (2013) Translational neuropsychiatry of genetic and neurodevelopmental animal models of schizophrenia. Revista de Psiquiatria Clinica, 40 (1). pp. 41-50.

Z

Zhu, Hong, Guariglia, Sara, Yu, Raymond Y.L., Li, Wenjing, Brancho, Deborah, Peinado, Hector, Lyden, David, Salzer, James, Bennett, Craig, and Chow, Chi-Wing (2013) Mutation of SIMPLE in Charcot-Marie-Tooth 1C alters production of exosomes. Molecular Biology of the Cell, 24 (11). pp. 1619-1637.