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Structural aspects of HDAC8 mechanism and dysfunction in Cornelia de Lange syndrome spectrum disorders

  • Published:2016-09-16 Issue:11 Volume:25 Page:1965-1976
  • ISSN:0961-8368
  • Container-title:Protein Science
  • language:en
  • Short-container-title:Protein Science

Author:

Deardorff Matthew A.12,Porter Nicholas J.3,Christianson David W.3

Affiliation:

1. Division of Human Genetics and Molecular Biology; The Children's Hospital of Philadelphia; Pennsylvania 19104

2. Department of Pediatrics, Perelman School of Medicine; University of Pennsylvania; Philadelphia Pennsylvania 19104

3. Roy and Diana Vagelos Laboratories, Department of Chemistry; University of Pennsylvania; Philadelphia PA 19104-6323

Funder

Doris Duke Charitable Foundation

National Institutes of Health

Publisher

Wiley

Subject

Molecular Biology,Biochemistry

Reference55 articles.

1. Cornelia de Lange syndrome, cohesin, and beyond;Liu;Clin Genet,2009

2. On the molecular etiology of Cornelia de Lange syndrome;Dorsett;Ann NY Acad Sci,2009

3. Cornelia de Lange syndrome;Liu;Adv Exp Med Biol,2010

4. Cornelia de Lange syndrome;Boyle;Clin Genet,2015

5. Descriptive epidemiology of Cornelia de Lange syndrome in Europe;Barisic;Am J Med Genet a,2008

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