Functional Characterization of a Novel GPC3 Missense Variant in Simpson-Golabi-Behmel Syndrome.

Zhao T, Allan K, Taylor J, Thorburn DR, White SM, Tan TY, Christodoulou J, Tan NB, Stroud DA

Open source

DOI
10.1002/ajmg.a.64287
Published
2026 Mar
Container
American journal of medical genetics. Part A
Publisher
Not recorded
Open access
unknown

Credibility signals

limited evidence Score 43/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.

Show all credibility signals

Cite this work

BibTeX

@article{allodium:10.1002/ajmg.a.64287,
  title = {Functional Characterization of a Novel GPC3 Missense Variant in Simpson-Golabi-Behmel Syndrome.},
  author = {Zhao T and Allan K and Taylor J and Thorburn DR and White SM and Tan TY and Christodoulou J and Tan NB and Stroud DA},
  year = {2026},
  journal = {American journal of medical genetics. Part A},
  doi = {10.1002/ajmg.a.64287},
  url = {https://doi.org/10.1002/ajmg.a.64287}
}

RIS

TY  - JOUR
TI  - Functional Characterization of a Novel GPC3 Missense Variant in Simpson-Golabi-Behmel Syndrome.
AU  - Zhao T
AU  - Allan K
AU  - Taylor J
AU  - Thorburn DR
AU  - White SM
AU  - Tan TY
AU  - Christodoulou J
AU  - Tan NB
AU  - Stroud DA
PY  - 2026
JO  - American journal of medical genetics. Part A
DO  - 10.1002/ajmg.a.64287
UR  - https://doi.org/10.1002/ajmg.a.64287
ER  - 

APA

T, Z., K, A., J, T., DR, T., SM, W., TY, T., J, C., NB, T., & DA, S. (2026). Functional Characterization of a Novel GPC3 Missense Variant in Simpson-Golabi-Behmel Syndrome.. American journal of medical genetics. Part A. https://doi.org/10.1002/ajmg.a.64287

Source records