Clinical and genetic analysis of Chinese patients with Leigh syndrome caused by biallelic loss-of-function variants of the NDUFAF6 gene.

Yang Q, Zhang Q, Zhou X, Qin Z, Liang X, Yi S, Zhang S, Lu W, Yi S, Luo J

Open source

DOI: 10.3389/fneur.2026.1778719
Published: 2026
Container: Frontiers in neurology
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.3389/fneur.2026.1778719,
  title = {Clinical and genetic analysis of Chinese patients with Leigh syndrome caused by biallelic loss-of-function variants of the NDUFAF6 gene.},
  author = {Yang Q and Zhang Q and Zhou X and Qin Z and Liang X and Yi S and Zhang S and Lu W and Yi S and Luo J},
  year = {2026},
  journal = {Frontiers in neurology},
  doi = {10.3389/fneur.2026.1778719},
  url = {https://doi.org/10.3389/fneur.2026.1778719}
}

RIS

TY  - JOUR
TI  - Clinical and genetic analysis of Chinese patients with Leigh syndrome caused by biallelic loss-of-function variants of the NDUFAF6 gene.
AU  - Yang Q
AU  - Zhang Q
AU  - Zhou X
AU  - Qin Z
AU  - Liang X
AU  - Yi S
AU  - Zhang S
AU  - Lu W
AU  - Yi S
AU  - Luo J
PY  - 2026
JO  - Frontiers in neurology
DO  - 10.3389/fneur.2026.1778719
UR  - https://doi.org/10.3389/fneur.2026.1778719
ER  -

APA

Q, Y., Q, Z., X, Z., Z, Q., X, L., S, Y., S, Z., W, L., S, Y., & J, L. (2026). Clinical and genetic analysis of Chinese patients with Leigh syndrome caused by biallelic loss-of-function variants of the NDUFAF6 gene.. Frontiers in neurology. https://doi.org/10.3389/fneur.2026.1778719

Source records

pubmed · retrieved 2026-09-26T05:22:27.744Z
europe-pmc · retrieved 2026-09-26T05:22:27.754Z
doaj · retrieved 2026-09-26T05:22:27.740Z