Varaico: Literature-Extracted Genetic Variants

Gene:FOXG1
Variant:p.I190N
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FOXG1

NM_005249.5:p.I190N

Associated Papers

Sleep Disorders in Rett Syndrome and Rett-Related Disorders: A Narrative Review.

Tascini G et al.

Frontiers in Neurology, 2022

FOXG1-Related Syndrome: From Clinical to Molecular Genetics and Pathogenic Mechanisms.

Wong LC et al.

International Journal of Molecular Sciences, 2019

31454984 (PubMed )
Supplement: ijms-20-04176-s001.pdf

Hypoplastic hippocampus in atypical Rett syndrome with a novel FOXG1 mutation.

Harada K et al.

Brain & Development, 2018

A case of congenital Rett variant in a Chinese patient caused by a FOXG1 mutation.

Niu Y et al.

Annals of Saudi Medicine, 0

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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."