Loss of SETDB1 decompacts the inactive X chromosome in part through reactivation of an enhancer in the IL1RAPL1 gene
Zhuo Sun(Florida State University), Brian P. Chadwick(Florida State University)
Cited by 16
Related Papers
Tissue-Specific Expression of a Splicing Mutation in the Gene Causes Familial Dysautonomia
|The American Journal of Human Genetics|2001|595