Varaico: Literature-Extracted Genetic Variants

Gene:PTPRQ
Variant:p.N2027insFs
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PTPRQ

NM_001145026.2:p.N2027insFs

Associated Papers

Novel PTPRQ variants associated with hearing loss in a Chinese family PTPRQ variants in Chinese hearing loss.

Hou Y et al.

Frontiers in Genetics, 2024

Delayed progressive sensorineural hearing loss due to a novel compound heterozygous PTPRQ mutation in a Chinese patient.

Qin Y et al.

Journal of Clinical Laboratory Analysis, 2023

Targeted Next-Generation Sequencing Identified Novel Compound Heterozygous Variants in the PTPRQ Gene Causing Autosomal Recessive Hearing Loss in a Chinese Family.

Jin Y et al.

Frontiers in Genetics, 2022

Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing.

Ammar-Khodja F et al.

Molecular Genetics & Genomic Medicine, 2015

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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."