Your browser doesn't support javascript.
loading
SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3.
Neurology ; 81(2): 165-73, 2013 Jul 09.
Article in En | MEDLINE | ID: mdl-23749797

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Charcot-Marie-Tooth Disease / Mutation, Missense / Intracellular Signaling Peptides and Proteins / Transcriptome Type of study: Etiology_studies / Prognostic_studies Limits: Adult / Female / Humans / Male / Middle aged Country/Region as subject: Asia Language: En Journal: Neurology Year: 2013 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Charcot-Marie-Tooth Disease / Mutation, Missense / Intracellular Signaling Peptides and Proteins / Transcriptome Type of study: Etiology_studies / Prognostic_studies Limits: Adult / Female / Humans / Male / Middle aged Country/Region as subject: Asia Language: En Journal: Neurology Year: 2013 Type: Article