Academic Journal
Corrigendum: Identification of the CFTR c.1666A > G mutation in hereditary inclusion body myopathy using next-generation sequencing analysis
| العنوان: | Corrigendum: Identification of the CFTR c.1666A > G mutation in hereditary inclusion body myopathy using next-generation sequencing analysis |
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| المؤلفون: | Lu, Yan, Da, Yu-Wei, Zhang, Yong-Biao, Li, Xin-Gang, Wang, Min, Di, Li, Pang, Mi, Lei, Lin |
| المصدر: | Research outputs 2014 to 2021 |
| بيانات النشر: | Edith Cowan University, Research Online, Perth, Western Australia |
| سنة النشر: | 2018 |
| المجموعة: | Edith Cowan University (ECU, Australia): Research Online |
| مصطلحات موضوعية: | hereditary inclusion body myopathy, next-generation sequencing, CFTR, mutation, whole-exome sequencing, Neurosciences |
| الوصف: | A Corrigendum on Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis by Lu, Y., Da, Y.-W., Zhang, Y.-B., Li, X.-G., Wang, M., Di, L., et al. (2018). Front. Neurosci. 12:329. doi:10.3389/fnins.2018.00329 An error was found in the first and second sentence of the original article's abstract. |
| نوع الوثيقة: | text |
| وصف الملف: | application/pdf |
| اللغة: | unknown |
| Relation: | https://ro.ecu.edu.au/ecuworkspost2013/5385; https://ro.ecu.edu.au/context/ecuworkspost2013/article/6392/viewcontent/fnins_12_00570.pdf |
| DOI: | 10.3389/fnins.2018.00570 |
| الاتاحة: | https://ro.ecu.edu.au/ecuworkspost2013/5385 https://doi.org/10.3389/fnins.2018.00570 https://ro.ecu.edu.au/context/ecuworkspost2013/article/6392/viewcontent/fnins_12_00570.pdf |
| Rights: | http://creativecommons.org/licenses/by/4.0/ |
| رقم الانضمام: | edsbas.AC8D5994 |
| قاعدة البيانات: | BASE |
| DOI: | 10.3389/fnins.2018.00570 |
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