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Genotype-Phenotype Correlations in Charcot-Marie-Tooth Disease Due to MTMR2 Mutations and Implications in Membrane Trafficking.
Wang, Haicui; Kaçar Bayram, Ayse; Sprute, Rosanne; Ozdemir, Ozkan; Cooper, Emily; Pergande, Matthias; Efthymiou, Stephanie; Nedic, Ivana; Mazaheri, Neda; Stumpfe, Katharina; Azizi Malamiri, Reza; Shariati, Gholamreza; Zeighami, Jawaher; Bayram, Nurettin; Naghibzadeh, Seyed Kianoosh; Tajik, Mohamad; Yasar, Mehmet; Sami Güven, Ahmet; Bibi, Farah; Sultan, Tipu; Salpietro, Vincenzo; Houlden, Henry; Per, Hüseyin; Galehdari, Hamid; Shalbafan, Bita; Jamshidi, Yalda; Cirak, Sebahattin.
Afiliación
  • Wang H; Department of Pediatrics, University Hospital Cologne, Cologne, Germany.
  • Kaçar Bayram A; Center for Molecular Medicine (CMMC), University of Cologne, Cologne, Germany.
  • Sprute R; Department of Pediatric Neurology, University of Health Sciences, Kayseri City Hospital, Kayseri, Turkey.
  • Ozdemir O; Department of Pediatrics, University Hospital Cologne, Cologne, Germany.
  • Cooper E; Center for Molecular Medicine (CMMC), University of Cologne, Cologne, Germany.
  • Pergande M; Department of Pediatrics, University Hospital Cologne, Cologne, Germany.
  • Efthymiou S; Center for Molecular Medicine (CMMC), University of Cologne, Cologne, Germany.
  • Nedic I; Genetics Research Centre, Molecular and Clinical Sciences Institute, St. George's, University of London, London, United Kingdom.
  • Mazaheri N; Department of Pediatrics, University Hospital Cologne, Cologne, Germany.
  • Stumpfe K; Center for Molecular Medicine (CMMC), University of Cologne, Cologne, Germany.
  • Azizi Malamiri R; Department of Neuromuscular Disorders, Institute of Neurology, University College London, London, United Kingdom.
  • Shariati G; Genetics Research Centre, Molecular and Clinical Sciences Institute, St. George's, University of London, London, United Kingdom.
  • Zeighami J; Narges Medical Genetics and Prenatal Diagnosis Laboratory, Ahvaz, Iran.
  • Bayram N; Department of Genetics, Faculty of Science, Shahid Chamran University of Ahvaz, Ahvaz, Iran.
  • Naghibzadeh SK; Department of Pediatrics, University Hospital Cologne, Cologne, Germany.
  • Tajik M; Paediatric Neurology, Department of Paediatric Neurology, Golestan Medical, Educational, and Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
  • Yasar M; Narges Medical Genetics and Prenatal Diagnosis Laboratory, Ahvaz, Iran.
  • Sami Güven A; Department of Medical Genetics, Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
  • Bibi F; Narges Medical Genetics and Prenatal Diagnosis Laboratory, Ahvaz, Iran.
  • Sultan T; Department of Ophthalmology, University of Health Sciences, Kayseri City Hospital, Kayseri, Turkey.
  • Salpietro V; Department of Medicine, Azad University, Tehran, Iran.
  • Houlden H; Department of Neurology, Firoozgar General Hospital, University of Medical Sciences, Tehran, Iran.
  • Per H; Department of Ear Nose and Throat, University of Health Sciences, Kayseri City Hospital, Kayseri, Turkey.
  • Galehdari H; Department of Pediatric Neurology, Meram Medical Faculty, Necmettin Erbakan University, Konya, Turkey.
  • Shalbafan B; Institute of Biochemistry and Biotechnology, PMAS Arid Agriculture University, Rawalpindi, Pakistan.
  • Jamshidi Y; Department of Pediatric Neurology, Institute of Child Health, The Children's Hospital Lahore, Lahore, Pakistan.
  • Cirak S; Department of Neuromuscular Disorders, Institute of Neurology, University College London, London, United Kingdom.
Front Neurosci ; 13: 974, 2019.
Article en En | MEDLINE | ID: mdl-31680794
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Front Neurosci Año: 2019 Tipo del documento: Article País de afiliación: Alemania
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Front Neurosci Año: 2019 Tipo del documento: Article País de afiliación: Alemania