Baets, Jonathan <br/><br/>
Defects of mutant DNMT1 are linked to a spectrum of neurological disorders.  [electronic resource] 

 -  Brain : a journal of neurology  Apr 2015 
 - 845-61 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1460-2156 
<br/><br/><label>Standard No.: </label>10.1093/brain/awv010  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Autophagy--genetics<br/>DNA (Cytosine-5-)-Methyltransferase 1<br/>DNA (Cytosine-5-)-Methyltransferases--chemistry<br/>Female<br/>HEK293 Cells<br/>Hereditary Sensory and Autonomic Neuropathies--diagnosis<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation--genetics<br/>Nervous System Diseases--diagnosis<br/>Pedigree<br/>Protein Structure, Secondary