Sage Journals: Discover world-class research

Free access

Research article

First published 2019-2

Frameshift mutation of candidate tumor suppressor genes QK1 and TMEFF2 in gastric and colorectal cancers

Ha Yoon Mo, Yun Sol Jo, Nam Jin Yoo [...]

Cancer Biomarkers

Retricted access

Case report

First published 2022-4

A Novel IRF6 Frameshift Mutation in a Large Chinese Pedigree With Van der Woude syndrome

Qi Peng, Wenyan Qin, Siping Li [...]

The Cleft Palate Craniofacial Journal

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Announcement

First published 2007-3

Dominant Optic Atrophy in a Japanese Family with Opa1 Frameshift Mutation (V942fsX966)

T. Hayashi, T. Takeuchi, T. Gekka [...]

European Journal of Ophthalmology

Open access

Research article

First published 2025-8

Inherited prion disease caused by a novel frameshift mutation of PRNP resulting in protein truncation at codon 157

Leah Holm-Mercer, Tze How Mok, Danielle Sequeira [...]

Journal of Alzheimer’s Disease

Free access

Research article

First published 2013-11

BaxΔ2 Family Alternative Splicing Salvages Bax Microsatellite-Frameshift Mutations

Bonnie Haferkamp, Honghong Zhang, Samuel Kissinger [...]

Genes & Cancer

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Research article

First published 2008-12

A Novel Frameshift Mutation in FRMD7 Causing X-Linked Idiopathic Congenital Nystagmus

Xiang He, Feng Gu, Ze Wang [...]

Genetic Testing and Molecular Biomarkers

Open access

Research article

First published 2021-05-04

In-Frame and Frameshift Mutations in Zebrafish Presenilin 2 Affect Different Cellular Functions in Young Adult Brains

Karissa Barthelson, Stephen Martin Pederson, Morgan Newman [...]

Journal of Alzheimer's Disease Reports

Open access

Case report

First published 2019

Identification of an HNF1A p.Gly292fs Frameshift Mutation Presenting as Diabetes During Pregnancy in a Maltese Family

Nikolai Paul Pace, Christopher Rizzo, Alexia Abela [...]

Clinical Medicine Insights: Case Reports

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Research article

First published 2018-03

Targeted Next-Generation Sequencing Reveals a Novel Frameshift Mutation in the MERTK Gene in a Chinese Family with Retinitis Pigmentosa

Mu Yang, Shujin Li, Wenjing Liu [...]

Genetic Testing and Molecular Biomarkers

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Research article

First published 2023-09

Two Novel Frameshift Mutations in the GLI3 Gene Underlie Non-Syndromic Polydactyly in Chinese Families

Xiaoyan Guo, Tengfei Shi, Mingrui Lin [...]

Genetic Testing and Molecular Biomarkers

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