Lattante, Serena <br/><br/>
Defining the association of TMEM106B variants among frontotemporal lobar degeneration patients with GRN mutations and C9orf72 repeat expansions.  [electronic resource] 

 -  Neurobiology of aging  Nov 2014 
 - 2658.e1-2658.e5 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1558-1497 
<br/><br/><label>Standard No.: </label>10.1016/j.neurobiolaging.2014.06.023  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Amyotrophic Lateral Sclerosis--complications<br/>C9orf72 Protein<br/>Cohort Studies<br/>Female<br/>France<br/>Frontotemporal Lobar Degeneration--complications<br/>Genetic Association Studies<br/>Genotype<br/>Humans<br/>Intercellular Signaling Peptides and Proteins--genetics<br/>Italy<br/>Male<br/>Membrane Proteins--genetics<br/>Middle Aged<br/>Mutation<br/>Nerve Tissue Proteins--genetics<br/>Polymorphism, Genetic<br/>Progranulins<br/>Proteins--genetics<br/>Trinucleotide Repeat Expansion--genetics