Novel Compound Heterozygous Variants in the TCTN2 Gene Causing Meckel-Gruber Syndrome 8 in a Non-Consanguineous Chinese Family.

Yang Q, He W, Zhang Q, Yi S, Zhou X, Zhang S, Yi S, Zhang Q, Luo J

DOI: 10.1002/mgg3.70160
Published: 2025 Dec
Container: Molecular genetics & genomic medicine
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1002/mgg3.70160,
  title = {Novel Compound Heterozygous Variants in the TCTN2 Gene Causing Meckel-Gruber Syndrome 8 in a Non-Consanguineous Chinese Family.},
  author = {Yang Q and He W and Zhang Q and Yi S and Zhou X and Zhang S and Yi S and Zhang Q and Luo J},
  year = {2025},
  journal = {Molecular genetics \& genomic medicine},
  doi = {10.1002/mgg3.70160},
  url = {https://doi.org/10.1002/mgg3.70160}
}

RIS

TY  - JOUR
TI  - Novel Compound Heterozygous Variants in the TCTN2 Gene Causing Meckel-Gruber Syndrome 8 in a Non-Consanguineous Chinese Family.
AU  - Yang Q
AU  - He W
AU  - Zhang Q
AU  - Yi S
AU  - Zhou X
AU  - Zhang S
AU  - Yi S
AU  - Zhang Q
AU  - Luo J
PY  - 2025
JO  - Molecular genetics & genomic medicine
DO  - 10.1002/mgg3.70160
UR  - https://doi.org/10.1002/mgg3.70160
ER  -

APA

Q, Y., W, H., Q, Z., S, Y., X, Z., S, Z., S, Y., Q, Z., & J, L. (2025). Novel Compound Heterozygous Variants in the TCTN2 Gene Causing Meckel-Gruber Syndrome 8 in a Non-Consanguineous Chinese Family.. Molecular genetics & genomic medicine. https://doi.org/10.1002/mgg3.70160

Source records

pubmed · retrieved 2026-09-24T18:47:42.697Z