Varaico: Literature-Extracted Genetic Variants

Gene:FOXP2
Variant:p.Q390delFs
Back to variants list

FOXP2

NM_014491.4:p.Q390delFs

Associated Papers

In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2.

Morison LD et al.

Journal of Medical Genetics, 2023

FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum.

Reuter MS et al.

Journal of Medical Genetics, 2017

Functional characterization of rare FOXP2 variants in neurodevelopmental disorder.

Estruch SB et al.

Journal of Neurodevelopmental Disorders, 2016

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

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."