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

January 1, 2011
Hum Mol Genet
https://pubmed.ncbi.nlm.nih.gov/21515589

This article is currently being updated. View its version on PubMed.

https://pubmed.ncbi.nlm.nih.gov/21515589

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