Harel Yoon syndrome: a novel mutation in ATAD3A gene and expansion of the clinical spectrum.

Tawfik CA, Zaitoun R, Farag AA

DOI: 10.1080/13816810.2023.2183223
Published: 2023 Jun
Container: Ophthalmic genetics
Publisher: Not recorded
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1080/13816810.2023.2183223,
  title = {Harel Yoon syndrome: a novel mutation in ATAD3A gene and expansion of the clinical spectrum.},
  author = {Tawfik CA and Zaitoun R and Farag AA},
  year = {2023},
  journal = {Ophthalmic genetics},
  doi = {10.1080/13816810.2023.2183223},
  url = {https://doi.org/10.1080/13816810.2023.2183223}
}

RIS

TY  - JOUR
TI  - Harel Yoon syndrome: a novel mutation in ATAD3A gene and expansion of the clinical spectrum.
AU  - Tawfik CA
AU  - Zaitoun R
AU  - Farag AA
PY  - 2023
JO  - Ophthalmic genetics
DO  - 10.1080/13816810.2023.2183223
UR  - https://doi.org/10.1080/13816810.2023.2183223
ER  -

APA

CA, T., R, Z., & AA, F. (2023). Harel Yoon syndrome: a novel mutation in ATAD3A gene and expansion of the clinical spectrum.. Ophthalmic genetics. https://doi.org/10.1080/13816810.2023.2183223

Source records

pubmed · retrieved 2026-11-10T15:53:15.301Z