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Hereditary peripheral neuropathies diagnosed by next-generation sequencing | Tidsskrift for Den norske legeforening
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Hereditary Neuropathy Foundation - Could you be 1 of the estimated 3300 patients in the US with the gene causing SORD Deficiency? You may have been diagnosed with CMT2, or distal hereditary
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Mutations in the SIGMAR1 gene cause a distal hereditary motor neuropathy phenotype mimicking ALS: Report of two novel variants - ScienceDirect
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Overview of the classification and genetics of hereditary peripheral neuropathies and rare unclassified forms | SpringerLink
![Figure 2 from A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathy | Semantic Scholar Figure 2 from A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathy | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/05b6edcfb9c597ce4555544064842bad7426dda2/8-Figure2-1.png)
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Brain on X: "Jacquier et al. describe a new homozygous variant in the COQ7 gene in a family with distal hereditary motor neuropathy. They show that the variant affects coenzyme Q10 production,
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