Common alleles of CMT2 and NRPE1 are major determinants of CHH methylation variation in Arabidopsis thaliana | PLOS Genetics
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Intermediate Charcot–Marie–Tooth disease: an electrophysiological reappraisal and systematic review | SpringerLink
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Progressive mitochondrial dysfunction is a common disease mechanism in different subtypes of Charcot-Marie-Tooth disease | UAntwerp - Faculty of Pharmaceutical, Biomedical and Veterinary Sciences
![Photographs of CMT2 Individuals with IGHMBP2 Mutations (A) Legs and... | Download Scientific Diagram Photographs of CMT2 Individuals with IGHMBP2 Mutations (A) Legs and... | Download Scientific Diagram](https://www.researchgate.net/publication/269096682/figure/fig6/AS:669629433270272@1536663506002/Photographs-of-CMT2-Individuals-with-IGHMBP2-Mutations-A-Legs-and-feet-of-family-A.png)
Photographs of CMT2 Individuals with IGHMBP2 Mutations (A) Legs and... | Download Scientific Diagram
![Diverse CMT2 neuropathies are linked to aberrant G3BP interactions in stress granules - ScienceDirect Diverse CMT2 neuropathies are linked to aberrant G3BP interactions in stress granules - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0092867422016294-fx1.jpg)
Diverse CMT2 neuropathies are linked to aberrant G3BP interactions in stress granules - ScienceDirect
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Disruption of genes associated with Charcot-Marie-Tooth type 2 lead to common behavioural, cellular and molecular defects in Caenorhabditis elegans | bioRxiv
MedRewind - Charcot-Marie-Tooth disease is classified under hereditary sensory and motor neuropathies that damage the peripheral nerves. Characteristic nerve biopsy appearance in CMT1 is - onion bulb appearance. Dejerine-sottas disease is also
![Severe atrophy of the intrinsic hand muscles of a patient with CMT2 who... | Download Scientific Diagram Severe atrophy of the intrinsic hand muscles of a patient with CMT2 who... | Download Scientific Diagram](https://www.researchgate.net/publication/26892086/figure/fig3/AS:203018734706710@1425414846691/Severe-atrophy-of-the-intrinsic-hand-muscles-of-a-patient-with-CMT2-who-carries-a.png)
Severe atrophy of the intrinsic hand muscles of a patient with CMT2 who... | Download Scientific Diagram
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Next-generation sequencing in Charcot–Marie–Tooth disease: opportunities and challenges | Nature Reviews Neurology
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Contiguous and stochastic CHH methylation patterns of plant DRM2 and CMT2 revealed by single-read methylome analysis | Genome Biology | Full Text
![A comparison of type 1 versus 2 charcot‐marie‐tooth in terms of gait analysis and clinical examination measures - 2018 - Developmental Medicine & Child Neurology - Wiley Online Library A comparison of type 1 versus 2 charcot‐marie‐tooth in terms of gait analysis and clinical examination measures - 2018 - Developmental Medicine & Child Neurology - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/456b18d8-1ebb-4c2b-a961-791e7e900538/dmcn68_14017-fig-0020-m.jpg)
A comparison of type 1 versus 2 charcot‐marie‐tooth in terms of gait analysis and clinical examination measures - 2018 - Developmental Medicine & Child Neurology - Wiley Online Library
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