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Peer-reviewedCC BYFrontiers in genetics

Case Report: McLeod syndrome caused by a nonsense variant c.484C > T (p.Gln162Ter) in the XK gene in a Chinese Han family

  1. 14 + 4 Medical Doctor Program, Chinese Academy of Medical Sciences and Peking Union Medical College , ,
  2. 2Department of Neurology, Peking Union Medical College Hospital , ,

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BibTeX
@article{dong2026case,
  title = {{Case Report: McLeod syndrome caused by a nonsense variant c.484C > T (p.Gln162Ter) in the XK gene in a Chinese Han family}},
  author = {Luochu Dong and Mange Liu and Ying Tan},
  journal = {Frontiers in genetics},
  year = {2026},
  month = oct,
  url = {https://europepmc.org/article/PMC/PMC13669088},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Case Report: McLeod syndrome caused by a nonsense variant c.484C > T (p.Gln162Ter) in the XK gene in a Chinese Han family
AU  - Luochu Dong
AU  - Mange Liu
AU  - Ying Tan
PY  - 2026
DA  - 2026/10/19
JO  - Frontiers in genetics
UR  - https://europepmc.org/article/PMC/PMC13669088
SN  - 1664-8021
ER  -