Research Output for Bartosz Kowalski
Note: The 2012, 2013, 2014, 2015 publications have not been audited.
Bartosz Kowalski may be from another institution or only recently joined Deakin University.
Kennerson, Marina L.*, Nicholson, Garth A.*, Kaler, Stephen G.*, Kowalski, Bartosz*, Mercer, Julian F. B., Tang, Jingrong*, Llanos, Roxana M., Chu, Shannon*, Takata, Reinaldo I.*, Speck-Martins, Carlos E.*, Baets, Jonathan*, Almeida-Souza, Leonardo*, Fischer, Dirk*, Timmerman, Vincent*, Taylor, Philip E., Scherer, Steven S.*, Ferguson, Toby A.*, Bird, Thomas D.*, De Jonghe, Peter*, Feely, Shawna M. E.*, Shy, Michael E.* and Garbern, James Y.* (2010) Missense mutations in the copper transporter gene ATP7A cause X-Linked distal hereditary motor neuropathy, American journal of human genetics, vol. 86, no. 3, pp. 342-352, Cell Press, Cambridge, Mass. [C1.1]
ERA journal ID: 15639 – Scopus EID: 2-s2.0-77649236039
Citation counts: Scopus - 15, Thomson - 20
DRO entry for this publication
No grants and/or consultancies found or audited – the 2014 HERDC financial return has not been completed or loaded as yet.
No completions found or audited.
- * Not a member of Deakin University at time of output.
DRO to publications collection last synchronised: Saturday 23rd May 2015 10:04pm