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Atypical Mowat-Wilson patient confirms the importance of the novel association between ZFHX1B/SIP1 and NuRD corepressor complex.
Verstappen, Griet; van Grunsven, Leo A; Michiels, Christine; Van de Putte, Tom; Souopgui, Jacob; Van Damme, Jozef; Bellefroid, Eric; Vandekerckhove, Joël; Huylebroeck, Danny.
Affiliation
  • Verstappen G; Laboratory of Molecular Biology (Celgen), Department of Human Genetics, KULeuven, B-3000 Leuven, Belgium.
Hum Mol Genet ; 17(8): 1175-83, 2008 Apr 15.
Article in En | MEDLINE | ID: mdl-18182442
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / RNA-Binding Proteins / Histone Deacetylases / Intellectual Disability / Nerve Tissue Proteins Type of study: Risk_factors_studies Limits: Animals / Humans Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2008 Document type: Article Affiliation country: Bélgica
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / RNA-Binding Proteins / Histone Deacetylases / Intellectual Disability / Nerve Tissue Proteins Type of study: Risk_factors_studies Limits: Animals / Humans Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2008 Document type: Article Affiliation country: Bélgica