Varaico: Literature-Extracted Genetic Variants

Gene:FSCN1
Variant:p.A349T
Back to variants list

FSCN1

NM_003088.4:p.A349T

Associated Papers

Insights Into the Emerging Role of Baf53b in Autism Spectrum Disorder.

Rowland ME et al.

Frontiers in Molecular Neuroscience, 2022

Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons.

Bell S et al.

American Journal of Human Genetics, 2019

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."