Your browser doesn't support javascript.
loading
Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span.
Yücel-Yilmaz, Didem; Yücesan, Emrah; Yalnizoglu, Dilek; Oguz, Kader Karli; Sagiroglu, Mahmut Samil; Özbek, Ugur; Serdaroglu, Esra; Bilgiç, Basar; Erdem, Sevim; Iseri, Sibel Aylin Ugur; Hanagasi, Hasmet; Gürvit, Hakan; Özgül, Riza Köksal; Dursun, Ali.
Affiliation
  • Yücel-Yilmaz D; Department of Pediatric Metabolism, Institute of Child Health, Hacettepe University, Turkey.
  • Yücesan E; Department of Genetics, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Turkey.
  • Yalnizoglu D; Department of Pediatric Neurology, Hacettepe University Faculty of Medicine, Turkey.
  • Oguz KK; Department of Radiology, Hacettepe University Faculty of Medicine, Turkey.
  • Sagiroglu MS; Informatics and Information Security Research Center, National Research Institute of Electronics and Cryptology, TÜBITAK, Turkey.
  • Özbek U; Department of Genetics, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Turkey.
  • Serdaroglu E; Department of Pediatric Neurology, Hacettepe University Faculty of Medicine, Turkey.
  • Bilgiç B; Behavioral Neurology and Movement Disorders Unit, Department of Neurology, Istanbul University Faculty of Medicine, Turkey.
  • Erdem S; Department of Neurology, Hacettepe University Faculty of Medicine, Turkey.
  • Iseri SAU; Department of Genetics, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Turkey.
  • Hanagasi H; Behavioral Neurology and Movement Disorders Unit, Department of Neurology, Istanbul University Faculty of Medicine, Turkey.
  • Gürvit H; Behavioral Neurology and Movement Disorders Unit, Department of Neurology, Istanbul University Faculty of Medicine, Turkey.
  • Özgül RK; Department of Pediatric Metabolism, Institute of Child Health, Hacettepe University, Turkey.
  • Dursun A; Department of Pediatric Metabolism, Hacettepe University Faculty of Medicine, Turkey. Electronic address: adursun@hacettepe.edu.tr.
Brain Dev ; 40(6): 458-464, 2018 Jun.
Article in En | MEDLINE | ID: mdl-29544888
Subject(s)
Key words
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spastic Paraplegia, Hereditary / Kinesins / Mutation Type of study: Prognostic_studies Limits: Adolescent / Adult / Female / Humans / Male Language: En Journal: Brain Dev Year: 2018 Document type: Article Affiliation country: Country of publication:
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spastic Paraplegia, Hereditary / Kinesins / Mutation Type of study: Prognostic_studies Limits: Adolescent / Adult / Female / Humans / Male Language: En Journal: Brain Dev Year: 2018 Document type: Article Affiliation country: Country of publication: