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MECP2 truncating mutations cause histone H4 hyperacetylation in Rett syndrome.
Wan, M; Zhao, K; Lee, S S; Francke, U.
Affiliation
  • Wan M; Department of Genetics and Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, CA 94305-5323, USA.
Hum Mol Genet ; 10(10): 1085-92, 2001 May 01.
Article in En | MEDLINE | ID: mdl-11331619
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Repressor Proteins / Chromosomal Proteins, Non-Histone / Histones / Rett Syndrome / DNA-Binding Proteins Limits: Female / Humans / Male Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2001 Document type: Article Affiliation country: United States Country of publication: United kingdom
Search on Google
Add to My VHL
Print
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Repressor Proteins / Chromosomal Proteins, Non-Histone / Histones / Rett Syndrome / DNA-Binding Proteins Limits: Female / Humans / Male Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2001 Document type: Article Affiliation country: United States Country of publication: United kingdom