[Corrigendum] Mitochondrial G8292A and C8794T mutations in patients with Niemann‑Pick disease type C

• Authors:
  • Shahin Maserrat
  • Fatemeh Sharifpanah
  • Leila Akbari
  • Seyed Hasan Tonekaboni
  • Parvaneh Karimzadeh
  • Mahmood Reza Asharafi
  • Safoura Mazrouei
  • Heinrich Sauer
  • Massoud Houshmand

• View Affiliations

  
  Affiliations: Department of Biology, Faculty of Science, Islamic Azad University, Damghan 3671639998, Iran, Department of Physiology, Faculty of Medicine, Justus Liebig University, D-35392 Giessen, Germany, Houshmand Genetic Diagnostics Laboratory, Taban Clinic, Tehran 1997844151, Iran, Department of Neurology, Faculty of Medicine, Shahid Beheshti University, Tehran 19839‑63113, Iran, Department of Neurology, Faculty of Medicine, Tehran University, Tehran 1417613151, Iran, Department of Cardiology, Clinic of Internal Medicine I, Friedrich Schiller University, D-07747 Jena, Germany, Department of Medical Biotechnology, National Institute of Genetic Engineering and Biotechnology, Tehran 14965/161, Iran
• Published online on: October 3, 2018     https://doi.org/10.3892/br.2018.1156
• Pages: 545-545

• Copyright : © Maserrat et al. This is an open access article distributed under the terms of Creative Commons Attribution License [CC BY 4.0].

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