Uner Tan syndrome caused by a homozygousTUBB2Bmutation affecting microtubule stability-Reference-Cited by-同舟云学术

Uner Tan syndrome caused by a homozygousTUBB2Bmutation affecting microtubule stability

Published:2016-12-23 Issue: Volume: Page:ddw383
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum. Mol. Genet.

Author:

Breuss Martin W.,Nguyen Thai,Srivatsan Anjana,Leca Ines,Tian Guoling,Fritz Tanja,Hansen Andi H.,Musaev Damir,McEvoy-Venneri Jennifer,James Kiely N.,Rosti Rasim O.,Scott Eric,Tan Uner,Kolodner Richard D.,Cowan Nicholas J.,Keays David A.,Gleeson Joseph G.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/26/2/258/10935409/ddw383.pdf

Reference61 articles.

1. Centrosomes, microtubules and neuronal development

2. Breuss M. Keays D.A. (2014) Nguyen L. Hippenmeyer S. (eds.), In Cellular and Molecular Control of Neuronal Migration. Springer Netherlands, Dordrecht, in press., pp. 75–96.

3. Neuronal migration disorders: from genetic diseases to developmental mechanisms

4. The Diverse Genetic Landscape of Neurodevelopmental Disorders

5. LIS1 and DCX: Implications for brain development and human disease in relation to microtubules;Reiner;Scientifica,2013

Cited by 13 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. Comprehensive analysis of two hotspot codons in the TUBB4B gene and associated phenotypes;Scientific Reports;2024-05-08

2. Clinical and Molecular Spectrum of Autosomal Recessive CA8‐Related Cerebellar Ataxia;Movement Disorders;2024-04-06

3. Cryo-EM structures of human α1B/βI+βIVb microtubules shed light on isoform specific assembly;2023-12-02

4. Case Report: Exome and RNA Sequencing Identify a Novel de novo Missense Variant in HNRNPK in a Chinese Patient With Au-Kline Syndrome;Frontiers in Genetics;2022-03-29

5. Neurodevelopmental Syndrome with Intellectual Disability, Speech Impairment, and Quadrupedia Is Associated with Glutamate Receptor Delta 2 Gene Defect;Cells;2022-01-25