Varaico: Literature-Extracted Genetic Variants

Gene:FOXI1
Variant:p.N161del1
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FOXI1

NM_012188.5:p.N161del1

Associated Papers

Reevaluation of Enlarged Vestibular Aqueduct.

Huang S et al.

Jama Otolaryngology-- Head & Neck Surgery, 2025

Clinical utility of exome sequencing in hearing loss: a retrospective cohort study.

Liu C et al.

Frontiers in Genetics, 2025

Utility and limitations of exome sequencing as a genetic diagnostic tool for children with hearing loss.

Sheppard S et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2018

29907799 (PubMed )
Supplement: 41436_2018_4_MOESM3_ESM.xlsx › variant-_capture___coverage

Molecular and functional studies of 4 candidate loci in Pendred syndrome and nonsyndromic hearing loss.

Cirello V et al.

Molecular and Cellular Endocrinology, 2012

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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."