Hall, D A <br/><br/>
PRNP H187R mutation associated with neuropsychiatric disorders in childhood and dementia.  [electronic resource] 

 -  Neurology  Apr 2005 
 - 1304-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>1526-632X 
<br/><br/><label>Standard No.: </label>10.1212/01.WNL.0000156911.70131.06  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Age of Onset<br/>Brain--metabolism<br/>Child<br/>DNA Mutational Analysis<br/>Dementia--complications<br/>Disease Progression<br/>Female<br/>Genetic Predisposition to Disease--genetics<br/>Genetic Testing<br/>Humans<br/>Intellectual Disability--complications<br/>Male<br/>Mental Disorders--complications<br/>Middle Aged<br/>Mutation--genetics<br/>Neurons--metabolism<br/>Pedigree<br/>Prion Diseases--complications<br/>Prions--genetics