Lemke, Johannes R <br/><br/>
Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy.  [electronic resource] 

 -  Neurology  06 2016 
 - 2171-8 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1526-632X 
<br/><br/><label>Standard No.: </label>10.1212/WNL.0000000000002740  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Cohort Studies<br/>Consanguinity<br/>Heterozygote<br/>Homozygote<br/>Humans<br/>Intellectual Disability--genetics<br/>Movement Disorders--genetics<br/>Mutation<br/>Nerve Tissue Proteins--genetics<br/>Oocytes<br/>Phenotype<br/>Receptors, N-Methyl-D-Aspartate--genetics<br/>Seizures--genetics<br/>Xenopus laevis