A point mutation in the ubiquitin-associated domain of SQSMT1 is sufficient to cause a Paget's disease-like disorder in mice

Author： Daroszewska Anna   van 't Hof Robert J.   Rojas Javier A.   Layfield Robert   Landao-Basonga Euphemie   Rose Lorraine   Rose Ken   Ralston Stuart H.  

Publisher： Oxford University Press

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.20, Iss.14, 2011-07, pp. : 2734-2744

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