Differences in peripheral neuropathy in xeroderma pigmentosum complementation groups A and D as evaluated by nerve conduction studies

BACKGROUND: Xeroderma pigmentosum (XP) is a rare autosomal recessive genetic disorder with defective DNA nucleotide excision repair and associated with a high frequency of skin cancer. Approximately 25% of patients develop progressive neurological degeneration. Complementation groups XP-A and XP-D a...

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Detalles Bibliográficos
Autores principales: Lehky, Tanya J., Sackstein, Paul, Tamura, Deborah, Quezado, Martha, Wu, Tianxia, Khan, Sikandar G., Patronas, Nicholas J., Wiggs, Edythe, Brewer, Carmen C., DiGiovanna, John J., Kraemer, Kenneth H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8501575/
https://www.ncbi.nlm.nih.gov/pubmed/34627174
http://dx.doi.org/10.1186/s12883-021-02414-2

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