Fernández-Ramos, Joaquín A <br/><br/>
[Experience in molecular diagnostic in hereditary neuropathies in a pediatric tertiary hospital].  [electronic resource] 

 -  Revista de neurologia  Dec 2015 
 - 490-8 p.  digital 
<br/><br/> Publication Type: English Abstract; Journal Article 
<br/><br/><label>ISSN: </label>1576-6578 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Cell Cycle Proteins--genetics<br/>Charcot-Marie-Tooth Disease--classification<br/>Child<br/>Child, Preschool<br/>Connexins--genetics<br/>Consanguinity<br/>Demyelinating Diseases--diagnosis<br/>Female<br/>GTP Phosphohydrolases--genetics<br/>Hereditary Sensory and Motor Neuropathy--diagnosis<br/>Hospitals, Pediatric--statistics & numerical data<br/>Humans<br/>Intracellular Signaling Peptides and Proteins--genetics<br/>Male<br/>Mitochondrial Proteins--genetics<br/>Molecular Diagnostic Techniques<br/>Myelin Proteins--genetics<br/>Nerve Tissue Proteins--genetics<br/>Retrospective Studies<br/>Roma--genetics<br/>Spain--epidemiology<br/>TRPV Cation Channels--genetics<br/>Tertiary Care Centers--statistics & numerical data<br/>Gap Junction beta-1 Protein