A Novel LINS1 Truncating Mutation in Autosomal Recessive Nonsyndromic Intellectual Disability-Reference-Cited by-同舟云学术

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A Novel LINS1 Truncating Mutation in Autosomal Recessive Nonsyndromic Intellectual Disability

Published:2020-05-18 Issue: Volume:11 Page:
ISSN:1664-0640
Container-title:Frontiers in Psychiatry
language:
Short-container-title:Front. Psychiatry

Author:

Muthusamy Babylakshmi,Bellad Anikha,Prasad Pramada,Bandari Aravind K.,Bhuvanalakshmi G.,Kiragasur R. M.,Girimaji Satish Chandra,Pandey Akhilesh

Funder

The Wellcome Trust DBT India Alliance

Department of Biotechnology , Ministry of Science and Technology

Publisher

Frontiers Media SA

Subject

Psychiatry and Mental health

Reference43 articles.

1. Prevalence of intellectual disability: a meta-analysis of population-based studies;Maulik;Res Dev Disabil,2011

2. The genetic basis of non-syndromic intellectual disability: a review;Kaufman;J Neurodev Disord,2010

3. Gene networks associated with non-syndromic intellectual disability;Lee;J Neurogenet,2018

4. Genetics of recessive cognitive disorders;Musante;Trends Genet,2014

5. Next-Generation Sequencing Reveals Novel Mutations in X-linked Intellectual Disability;Muthusamy;OMICS,2017

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Domain‐specific phenotypes in LINS1‐related disorder—A Chinese family with the Q92X variant and literature review;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2024-04-02

2. Emerging Epidemiological Data on Rare Intellectual Disability Syndromes from Analyzing the Data of a Large Iranian Cohort;Archives of Iranian Medicine;2023-04-01

3. Identification of a novel nonsense homozygous mutation of LINS1 gene in two sisters with intellectual disability, schizophrenia, and anxiety;Biomedical Journal;2021-08

4. Non-Syndromic Intellectual Disability and Its Pathways: A Long Noncoding RNA Perspective;Non-Coding RNA;2021-03-11

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