TBC1D24truncating mutation resulting in severe neurodegeneration-Reference-Cited by-同舟云学术

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TBC1D24truncating mutation resulting in severe neurodegeneration

Published:2013-01-23 Issue:3 Volume:50 Page:199-202
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:J Med Genet

Author:

Guven Ayse,Tolun Aslıhan

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Cited by 67 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. V-ATPase Dysfunction in the Brain: Genetic Insights and Therapeutic Opportunities;Cells;2024-08-28

2. Ursids evolved dietary diversity without major alterations in metabolic rates;Scientific Reports;2024-02-27

3. Investigation of a novel TBC1D24 variation causing autosomal dominant non-syndromic hearing loss;Scientific Reports;2024-02-27

4. A Rare Cause of Paroxysmal Movement Disorder Associated with TBC1D24 Gene Mutation in Two Siblings;Annals of Indian Academy of Neurology;2023

5. Synaptic genes and neurodevelopmental disorders: From molecular mechanisms to developmental strategies of behavioral testing;Neurobiology of Disease;2022-10

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