-
Evans-Galea, MV, Corben, LA, Hasell, J, Galea, CA, Fahey, MC, du Sart, D, Delatycki, MB.
A novel deletion–insertion mutation identified in exon 3 of FXN in two siblings with a severe Friedreich ataxia phenotype.
neurogenetics
12(4)
:
307 -313
2011
view publication
-
Kelly, M, Bagnall, RD, Peverill, RE, Donelan, L, Corben, L, Delatycki, MB, Semsarian, C.
A polymorphic miR-155 binding site in AGTR1 is associated with cardiac hypertrophy in Friedreich ataxia.
Journal of Molecular and Cellular Cardiology
51(5)
:
848 -854
2011
view publication
-
Bertalli, NA, Allen, KJ, McLaren, CE, Turkovic, L, Osborne, NJ, Constantine, CC, Delatycki, MB, English, DR, Giles, GG, Hopper, JL, et al.
A comparison of self‐reported and record‐linked blood donation history in an Australian cohort.
Transfusion
51(10)
:
2189 -2198
2011
view publication
-
Liu, J, Verma, PJ, Evans-Galea, MV, Delatycki, MB, Michalska, A, Leung, J, Crombie, D, Sarsero, JP, Williamson, R, Dottori, M, et al.
Generation of Induced Pluripotent Stem Cell Lines from Friedreich Ataxia Patients.
Stem Cell Reviews and Reports
7(3)
:
703 -713
2011
view publication
-
Wang, Y, Gurrin, L, Wluka, A, Bertalli, N, Osborne, N, Delatycki, M, Giles, G, English, D, Hopper, J, Simpson, J, et al.
350 HFE C282Y HOMOZYGOSITY IS ASSOCIATED WITH AN INCREASED RISK OF TOTAL HIP REPLACEMENT FOR OSTEOARTHRITIS IN MEN BUT NOT WOMEN.
Osteoarthritis and Cartilage
19:
s158
2011
view publication