Now at Monash Institute for Medical Research, Melbourne, VIC 3168, Australia.
Next-generation sequencing in molecular diagnosis: NUBPL mutations highlight the challenges of variant detection and interpretation†
Version of Record online: 22 DEC 2011
© 2011 Wiley Periodicals, Inc.
Volume 33, Issue 2, pages 411–418, February 2012
How to Cite
Tucker, E. J., Mimaki, M., Compton, A. G., McKenzie, M., Ryan, M. T. and Thorburn, D. R. (2012), Next-generation sequencing in molecular diagnosis: NUBPL mutations highlight the challenges of variant detection and interpretation. Hum. Mutat., 33: 411–418. doi: 10.1002/humu.21654
Communicated by Mario Tosi
- Issue online: 12 JAN 2012
- Version of Record online: 22 DEC 2011
- Accepted manuscript online: 9 NOV 2011 11:27AM EST
- Manuscript Accepted: 31 OCT 2011
- Manuscript Received: 3 JUN 2011
- Australian National Health and Medical Research Council [NHMRC] (to M.M., M.T.R., and D.R.T.)
- Ramaciotti Foundation and the James and Vera Lawson Trust (to M.M.)
- Victorian Government's Operational Infrastructure Support Program (to D.R.T.)
- NHMRC Principal Research Fellowship (to D.R.T.)
- NHMRC Career Development Award (to M.M.)
- Australian Postgraduate Award (to E.J.T.)
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