Varaico: Literature-Extracted Genetic Variants

Gene:FOXP1
Variant:p.A532E
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FOXP1

NM_001349338.3:p.A532E

Associated Papers

A Comprehensive Study of De Novo Mutations on the Protein-Protein Interaction Interfaces Provides New Insights into Developmental Delay.

Maharjan DT et al.

Biomolecules, 2022

36358993 (PubMed )
Supplement: biomolecules-12-01643-s001.zip › Supplemental_Table_S2____PsychiPPI_in_developmental_delay.xlsx › Sheet1

Targeting extracellular and juxtamembrane FGFR2 mutations in chemotherapy-refractory cholangiocarcinoma.

Bitzer M et al.

Npj Precision Oncology, 2021

34480077 (PubMed )
Supplement: 41698_2021_220_MOESM1_ESM.pdf

Pathogenic missense mutation pattern of forkhead box genes in neurodevelopmental disorders.

Han L et al.

Molecular Genetics & Genomic Medicine, 2019

Prospective investigation of FOXP1 syndrome.

Siper PM et al.

Molecular Autism, 2017

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."