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Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes.
Nat Genet. 2020 May;52(5):473-481. doi: 10.1038/s41588-020-0615-4. Epub 2020 May 4.
Nat Genet. 2020.
PMID: 32367058
Free PMC article.
Charcot-Marie-Tooth disease and related disorders: an evolving landscape.
Laurá M, Pipis M, Rossor AM, Reilly MM.
Laurá M, et al.
Curr Opin Neurol. 2019 Oct;32(5):641-650. doi: 10.1097/WCO.0000000000000735.
Curr Opin Neurol. 2019.
PMID: 31343428
Review.
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Loss of BICD2 in muscle drives motor neuron loss in a developmental form of spinal muscular atrophy.
Rossor AM, Sleigh JN, Groves M, Muntoni F, Reilly MM, Hoogenraad CC, Schiavo G.
Rossor AM, et al.
Acta Neuropathol Commun. 2020 Mar 17;8(1):34. doi: 10.1186/s40478-020-00909-6.
Acta Neuropathol Commun. 2020.
PMID: 32183910
Free PMC article.
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