Coppola, Cinzia <br/><br/>
A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlations.  [electronic resource] 

 -  Neurobiology of aging  01 2017 
 - 219.e5-219.e13 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1558-1497 
<br/><br/><label>Standard No.: </label>10.1016/j.neurobiolaging.2016.10.008  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Alleles<br/>Female<br/>Founder Effect<br/>Frontotemporal Lobar Degeneration--genetics<br/>Gene Deletion<br/>Gene Dosage<br/>Genes, Dominant--genetics<br/>Genetic Association Studies<br/>Haplotypes<br/>Humans<br/>Intercellular Signaling Peptides and Proteins--blood<br/>Italy<br/>Male<br/>Middle Aged<br/>Multigene Family--genetics<br/>Mutation--genetics<br/>Progranulins<br/>Sequence Analysis, DNA<br/>Tandem Repeat Sequences