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A point mutation in the ubiquitin-associated domain of SQSMT1 is sufficient to cause a Paget's disease-like disorder in mice
Daroszewska, A., van 't Hof, R. J., Rojas, J. A., Layfield, R., Landao-Basonga, E., Rose, L., Rose, K., Ralston, S. H.Volume:
20
Language:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/ddr172
Date:
July, 2011
File:
PDF, 542 KB
english, 2011