Correction to "A Case of CSNK2A1 Gene Variant Causing Okur-Chung Syndrome and Analysis of the Clinical Phenotypic Spectrum".

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DOI: 10.1002/mgg3.70280
Published: 2026 Aug
Container: Molecular genetics & genomic medicine
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1002/mgg3.70280,
  title = {Correction to "A Case of CSNK2A1 Gene Variant Causing Okur-Chung Syndrome and Analysis of the Clinical Phenotypic Spectrum".},
  year = {2026},
  journal = {Molecular genetics \& genomic medicine},
  doi = {10.1002/mgg3.70280},
  url = {https://doi.org/10.1002/mgg3.70280}
}

RIS

TY  - JOUR
TI  - Correction to "A Case of CSNK2A1 Gene Variant Causing Okur-Chung Syndrome and Analysis of the Clinical Phenotypic Spectrum".
PY  - 2026
JO  - Molecular genetics & genomic medicine
DO  - 10.1002/mgg3.70280
UR  - https://doi.org/10.1002/mgg3.70280
ER  -

APA

Correction to "A Case of CSNK2A1 Gene Variant Causing Okur-Chung Syndrome and Analysis of the Clinical Phenotypic Spectrum".. (2026). Molecular genetics & genomic medicine. https://doi.org/10.1002/mgg3.70280

Source records

pubmed · retrieved 2026-09-27T11:44:24.367Z