Original language | English |
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Pages (from-to) | 2172-2180 |
Journal | Human Molecular Genetics |
Volume | 17 |
Issue number | 14 |
Publication status | Published - 2008 |
Publication type | A1 Journal article-refereed |
The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity.
M Gordillo, H Vega, AH Trainer, KOJ Simola
Research output: Contribution to journal › Article › Scientific › peer-review
99
Citations
(Scopus)