The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity

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  2. Dr Alison Trainer
Author(s)Gordillo M, Vega H, Trainer AH, Hou F, Sakai N, Luque R, Kayserili H, Basaran S, Skovby F, Hennekam RCM, Uzielli MLG, Schnur RE, Manouvrier S, Chang S, Blair E, Hurst JA, Forzano F, Meins M, Simola KOJ, Raas-rothschild A, Schultz RA, Mcdaniel LD, Ozono K, Inui K, Zou H, Jabs EW
Publication type Article
JournalHuman Molecular Genetics
Year2008
Volume17
Issue14
Pages2172-2180
ISSN (print)0964-6906
ISSN (electronic)1460-2083
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PublisherOxford University Press
URLhttp://dx.doi.org/10.1093/hmg/ddn116
DOI10.1093/hmg/ddn116
PubMed id18411254
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