<i>De novo</i> mutation in the <i>ARHGAP32</i> gene endorses the implication of GTPase-activating proteins (RhoGAP family) in idiopathic autism spectrum disorder.

Cirnigliaro L, Saccuzzo L, Marzà V, Randazzo M, Perdichizzi M, Romano C, Fichera M, Rizzo R, Barone R.

Open source

DOI
10.3389/fpsyt.2026.1754241
Published
2026-02-06
Container
Front Psychiatry
Publisher
Not recorded
Open access
yes

Credibility signals

uncertain Score 53/100 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:10.3389/fpsyt.2026.1754241,
  title = {\<i\>De novo\</i\> mutation in the \<i\>ARHGAP32\</i\> gene endorses the implication of GTPase-activating proteins (RhoGAP family) in idiopathic autism spectrum disorder.},
  author = {Cirnigliaro L and  Saccuzzo L and  Marzà V and  Randazzo M and  Perdichizzi M and  Romano C and  Fichera M and  Rizzo R and  Barone R.},
  year = {2026},
  journal = {Front Psychiatry},
  doi = {10.3389/fpsyt.2026.1754241},
  url = {https://doi.org/10.3389/fpsyt.2026.1754241}
}

RIS

TY  - JOUR
TI  - <i>De novo</i> mutation in the <i>ARHGAP32</i> gene endorses the implication of GTPase-activating proteins (RhoGAP family) in idiopathic autism spectrum disorder.
AU  - Cirnigliaro L
AU  -  Saccuzzo L
AU  -  Marzà V
AU  -  Randazzo M
AU  -  Perdichizzi M
AU  -  Romano C
AU  -  Fichera M
AU  -  Rizzo R
AU  -  Barone R.
PY  - 2026
JO  - Front Psychiatry
DO  - 10.3389/fpsyt.2026.1754241
UR  - https://doi.org/10.3389/fpsyt.2026.1754241
ER  - 

APA

L, C., L, S., V, M., M, R., M, P., C, R., M, F., R, R., & R., B. (2026). <i>De novo</i> mutation in the <i>ARHGAP32</i> gene endorses the implication of GTPase-activating proteins (RhoGAP family) in idiopathic autism spectrum disorder.. Front Psychiatry. https://doi.org/10.3389/fpsyt.2026.1754241

Source records