Scoles, D R <br/><br/>
A missense mutation in the neurofibromatosis 2 gene occurs in patients with mild and severe phenotypes.  [electronic resource] 

 -  Neurology  Aug 1996 
 - 544-6 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0028-3878 
<br/><br/><label>Standard No.: </label>10.1212/wnl.47.2.544  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Chromosome Mapping<br/>Genes, Neurofibromatosis 2--genetics<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation<br/>Neurofibromatosis 2--genetics<br/>Phenotype<br/>Polymorphism, Single-Stranded Conformational