Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Editorial
. 2021 Apr;28(4):1104-1105.
doi: 10.1111/ene.14734. Epub 2021 Feb 1.

Broadening the genetic spectrum of distal hereditary motor neuropathy

Alexander M Rossor  1
Affiliations
Editorial

Broadening the genetic spectrum of distal hereditary motor neuropathy

Alexander M Rossor. Eur J Neurol. 2021 Apr.
No abstract available

PubMed Disclaimer

Comment on

  • Distal hereditary motor neuropathies: Mutation spectrum and genotype-phenotype correlation.
    Frasquet M, Rojas-García R, Argente-Escrig H, Vázquez-Costa JF, Muelas N, Vílchez JJ, Sivera R, Millet E, Barreiro M, Díaz-Manera J, Turon-Sans J, Cortés-Vicente E, Querol L, Ramírez-Jiménez L, Martínez-Rubio D, Sánchez-Monteagudo A, Espinós C, Sevilla T, Lupo V. Frasquet M, et al. Eur J Neurol. 2021 Apr;28(4):1334-1343. doi: 10.1111/ene.14700. Epub 2021 Jan 10. Eur J Neurol. 2021. PMID: 33369814

References

REFERENCES

    1. Frasquet, M, Rojas-Garcia, R, Argente-Escrig, H, et al. Distal hereditary motor neuropathies: Mutation spectrum and genotype-phenotype correlation. Eur J Neurol. 2021.
    1. Bansagi B, Griffin H, Whittaker RG, et al. Genetic heterogeneity of motor neuropathies. Neurology. 2017;88(13):1226-1234.
    1. Syriani E, Morales M, Gamez J. The p. E22G mutation in the Cu/Zn superoxide-dismutase gene predicts a long survival time. J Neurol Sci. 2009;285(1-2):46-53.
    1. Cortese A, Zhu YI, Rebelo AP, et al. Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes. Nat Genet. 2020;52(5):473-481.
    1. Drew AP, Cutrupi AN, Brewer MH, Nicholson GA, Kennerson ML. A 1.35 Mb DNA fragment is inserted into the DHMN1 locus on chromosome 7q34-q36.2. Hum Genet. 2016;135(11):1269-1278.

MeSH terms

LinkOut - more resources