Duong, Linh <br/><br/>
Mutations in NRXN1 in a family multiply affected with brain disorders: NRXN1 mutations and brain disorders.  [electronic resource] 

 -  American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics  Apr 2012 
 - 354-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1552-485X 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.b.32036  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Base Sequence<br/>Brain Diseases--genetics<br/>Calcium-Binding Proteins<br/>Cell Adhesion Molecules, Neuronal--genetics<br/>Child<br/>Child, Preschool<br/>DNA Mutational Analysis<br/>Exons--genetics<br/>Family<br/>Female<br/>Genetic Predisposition to Disease<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Introns--genetics<br/>Male<br/>Molecular Sequence Data<br/>Mutation--genetics<br/>Nerve Tissue Proteins--genetics<br/>Neural Cell Adhesion Molecules<br/>Pedigree<br/>Phenotype