Clinical and Molecular Features of POLG-Related Sensory Ataxic Neuropathy with Dysarthria and Ophthalmoparesis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s12031-021-01831-9.pdf
Reference26 articles.
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2. Bereau M, Anheim M, Echaniz-Laguna A et al (2016) The wide POLG-related spectrum: An integrated view. J Neurol Sci 368:70–76
3. Bostan A, Glibert G, Dachy B, Dan B (2012) Novel mutation in spacer region of POLG associated with ataxia neuropathy spectrum and gastroparesis. Auton Neurosci 170:70–72
4. Da Pozzo P, Cardaioli E, Rubegni A et al (2017) Novel POLG mutations and variable clinical phenotypes in 13 Italian patients. Neurol Sci 38:563–570
5. Dong HL, Wei Q, Li JQ, Li HF, Bai G, Ma H, Wu ZY (2020) Genetic spectrum of MCM3AP and its relationship with phenotype of Charcot-Marie-Tooth disease. J Peripher Nerv Syst 25:107–111
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