Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

CYP17A1 intron mutation causing cryptic splicing in 17a-hydroxylase deficiency.

CYP17A1 intron mutation causing cryptic splicing in 17a-hydroxylase deficiency. PLoS One. 2011; 6(9):e25492.

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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.