A novel c.973G>T mutation in the ε-subunit of the acetylcholine receptor causing congenital myasthenic syndrome in an iranian family
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28. Aug. 2019
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Artikel-Kategorie: Case Report
Online veröffentlicht: 28. Aug. 2019
Seitenbereich: 95 - 98
DOI: https://doi.org/10.2478/bjmg-2019-0010
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© 2019 Karimzadeh P, Parvizi Omran S, Ghaedi H, Omrani MD, published by Sciendo
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
Karimzadeh, P
Pediatric Neurology Research Center, Research Institute for Children's Health, Shahid Beheshti University of Medical SciencesTehran, Islamic Republic of Iran
Department of Pediatric Neurology, Mofid Children's Hospital, Faculty of Medicine, Shahid Beheshti University of Medical SciencesTehran, Islamic Republic of Iran
Parvizi Omran, S
Department of Biology, Damghan Branch, Islamic Azad UniversityDamghan, Islamic Republic of Iran
Ghaedi, H
Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical SciencesTehran, Islamic Republic of Iran
Omrani, MD
Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical SciencesTehran, Islamic Republic of Iran