دورية أكاديمية
Heterozygous POLG variant Ser1181Asn is associated with autosomal dominant neuro-myopathy in one family with no further specific manifestations of mitochondrial syndrome
العنوان: | Heterozygous POLG variant Ser1181Asn is associated with autosomal dominant neuro-myopathy in one family with no further specific manifestations of mitochondrial syndrome |
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المؤلفون: | Maike F. Dohrn, Danique Beijer, Lejla Mulahasanovic |
المصدر: | Neurological Research and Practice, Vol 4, Iss 1, Pp 1-2 (2022) |
بيانات النشر: | BMC, 2022. |
سنة النشر: | 2022 |
المجموعة: | LCC:Neurosciences. Biological psychiatry. Neuropsychiatry LCC:Neurology. Diseases of the nervous system |
مصطلحات موضوعية: | Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571, Neurology. Diseases of the nervous system, RC346-429 |
نوع الوثيقة: | article |
وصف الملف: | electronic resource |
اللغة: | English |
تدمد: | 2524-3489 |
العلاقة: | https://doaj.org/toc/2524-3489Test |
DOI: | 10.1186/s42466-022-00197-6 |
الوصول الحر: | https://doaj.org/article/254293be02574a4f81f860de7a42527fTest |
رقم الانضمام: | edsdoj.254293be02574a4f81f860de7a42527f |
قاعدة البيانات: | Directory of Open Access Journals |
تدمد: | 25243489 |
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DOI: | 10.1186/s42466-022-00197-6 |