AAV-mediated CBLN1 replacement rescues hereditary ataxia caused by biallelic CBLN1 variants.

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Last updated 9/4/2026, 12:24:16 AM

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African DSI DataBank. AAV-mediated CBLN1 replacement rescues hereditary ataxia caused by biallelic CBLN1 variants.. AFDSI-PUB-943. 2026. https://hub.africandsidatabank.africa/cite/AFDSI-PUB-943 Mirrored from data source: PubMed: https://pubmed.ncbi.nlm.nih.gov/42687380/.

BibTeX
@misc{AFDSIPUB943,
  title        = {AAV-mediated CBLN1 replacement rescues hereditary ataxia caused by biallelic CBLN1 variants.},
  author       = {{African DSI DataBank}},
  year         = {2026},
  howpublished = {\url{https://hub.africandsidatabank.africa/cite/AFDSI-PUB-943}},
  note         = {African DSI DataBank citable identifier AFDSI-PUB-943; Mirrored from data source: PubMed: https://pubmed.ncbi.nlm.nih.gov/42687380/}
}

AFDSI-PUB-943 is a stable, resolvable local identifier — not a registered DOI. See Terms of use's "Citation policy" for the full explanation.