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

Lookup NU author(s): Dr Alison Trainer

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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

Journal: Human Molecular Genetics

Year: 2008

Volume: 17

Issue: 14

Pages: 2172-2180

Print publication date: 01/07/2008

ISSN (print): 0964-6906

ISSN (electronic): 1460-2083

Publisher: Oxford University Press

URL: http://dx.doi.org/10.1093/hmg/ddn116

DOI: 10.1093/hmg/ddn116

PubMed id: 18411254


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