Tian, Yun <br/><br/>
Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders.  [electronic resource] 

 -  American journal of human genetics  07 2019 
 - 166-176 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1537-6605 
<br/><br/><label>Standard No.: </label>10.1016/j.ajhg.2019.05.013  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Female<br/>Humans<br/>Intranuclear Inclusion Bodies--genetics<br/>Male<br/>Middle Aged<br/>Neurodegenerative Diseases--genetics<br/>Pedigree<br/>Receptors, Notch--genetics<br/>Trinucleotide Repeat Expansion--genetics<br/>Exome Sequencing