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

Author:

Masserrat Abbas1,Sharifpanah Fatemeh2,Akbari Leila3,Tonekaboni Seyed4,Karimzadeh Parvaneh4,Asharafi Mahmood Reza5,Mazouei Safoura6,Sauer Heinrich2,Houshmand Massoud7

Affiliation:

1. Department of Biology, Faculty of Science, Islamic Azad University, Damghan 3671639998, Iran

2. Department of Physiology, Faculty of Medicine, Justus Liebig University, D-35392 Giessen, Germany

3. Houshmand Genetic Diagnostics Laboratory, Taban Clinic, Tehran 1997844151, Iran

4. Department of Neurology, Faculty of Medicine, Shahid Beheshti University, Tehran 19839‑63113, Iran

5. Department of Neurology, Faculty of Medicine, Tehran University, Tehran 1417613151, Iran

6. Department of Cardiology, Clinic of Internal Medicine I, Friedrich Schiller University, D-07747 Jena, Germany

7. Department of Medical Biotechnology, National Institute of Genetic Engineering and Biotechnology, Tehran 14965/161, Iran

Publisher

Spandidos Publications

Subject

General Pharmacology, Toxicology and Pharmaceutics,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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