Verstappen, Griet <br/><br/>
Atypical Mowat-Wilson patient confirms the importance of the novel association between ZFHX1B/SIP1 and NuRD corepressor complex.  [electronic resource] 

 -  Human molecular genetics  Apr 2008 
 - 1175-83 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1460-2083 
<br/><br/><label>Standard No.: </label>10.1093/hmg/ddn007  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--metabolism<br/>Adenosine Triphosphatases--metabolism<br/>Animals<br/>Autoantigens--metabolism<br/>Cadherins--metabolism<br/>Cell Line<br/>DNA Helicases--metabolism<br/>Embryo, Nonmammalian--metabolism<br/>Histone Deacetylases--metabolism<br/>Humans<br/>Intellectual Disability--metabolism<br/>Mi-2 Nucleosome Remodeling and Deacetylase Complex<br/>Nerve Tissue Proteins--chemistry<br/>Protein Structure, Tertiary<br/>RNA-Binding Proteins--chemistry<br/>Syndrome<br/>Xenopus