Familial Moyamoya disease associated with dual RNF213 variants (R4810K and T1727M): A case report and genetic investigation.

Sang B, Lu W, Feng L.

DOI: 10.1097/md.0000000000047079
Published: 2026-01-01
Container: Medicine (Baltimore)
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1097/md.0000000000047079,
  title = {Familial Moyamoya disease associated with dual RNF213 variants (R4810K and T1727M): A case report and genetic investigation.},
  author = {Sang B and  Lu W and  Feng L.},
  year = {2026},
  journal = {Medicine (Baltimore)},
  doi = {10.1097/md.0000000000047079},
  url = {https://doi.org/10.1097/md.0000000000047079}
}

RIS

TY  - JOUR
TI  - Familial Moyamoya disease associated with dual RNF213 variants (R4810K and T1727M): A case report and genetic investigation.
AU  - Sang B
AU  -  Lu W
AU  -  Feng L.
PY  - 2026
JO  - Medicine (Baltimore)
DO  - 10.1097/md.0000000000047079
UR  - https://doi.org/10.1097/md.0000000000047079
ER  -

APA

B, S., W, L., & L., F. (2026). Familial Moyamoya disease associated with dual RNF213 variants (R4810K and T1727M): A case report and genetic investigation.. Medicine (Baltimore). https://doi.org/10.1097/md.0000000000047079

Source records

europe-pmc · retrieved 2026-09-26T08:23:25.751Z