Varaico: Literature-Extracted Genetic Variants

Gene:ICOS
Variant:p.F108_L111delFs
Back to variants list

ICOS

NM_012092.4:p.F108_L111delFs

Associated Papers

Expanding Clinical Phenotype and Novel Insights into the Pathogenesis of ICOS Deficiency.

Abolhassani H et al.

Journal of Clinical Immunology, 2020

Evaluating the Genetics of Common Variable Immunodeficiency: Monogenetic Model and Beyond.

de Valles-Ibáñez G et al.

Frontiers in Immunology, 2018

29867916 (PubMed )
Supplement: data_sheet_1.PDF

14 Years after Discovery: Clinical Follow-up on 15 Patients with Inducible Co-Stimulator Deficiency.

Schepp J et al.

Frontiers in Immunology, 2017

Astute Clinician Report: A Novel 10 bp Frameshift Deletion in Exon 2 of ICOS Causes a Combined Immunodeficiency Associated with an Enteritis and Hepatitis.

Robertson N et al.

Journal of Clinical Immunology, 2015

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."