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

标题
A point mutation in the ubiquitin-associated domain of SQSMT1 is sufficient to cause a Paget's disease-like disorder in mice
作者
关键词
-
出版物
HUMAN MOLECULAR GENETICS
Volume 20, Issue 14, Pages 2734-2744
出版商
Oxford University Press (OUP)
发表日期
2011-04-23
DOI
10.1093/hmg/ddr172

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