The 1316T>C missenses mutation in MTHFR contributes to MTHFR deficiency by targeting MTHFR to proteasome degradation-Reference-Cited by-同舟云学术

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The 1316T>C missenses mutation in MTHFR contributes to MTHFR deficiency by targeting MTHFR to proteasome degradation

Published:2020-12-03 Issue:1 Volume:13 Page:1176-1185
ISSN:1945-4589
Container-title:Aging
language:en
Short-container-title:Aging

Author:

Liu Xi¹,Li Yu²³,Wang Menghan¹,Wang Xiaojun¹,Zhang Limin¹,Peng Tao¹,Liang Wenping²³,Wang Zhe²³,Lu Hong¹

Affiliation:

1. Department of Neurology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China

2. The National Clinical Research Center for Geriatric Disease, Xuanwu Hospital, Capital Medical University, Beijing 100053, China

3. Advanced Innovation Center for Human Brain Protection, Capital Medical University, Beijing 100053, China

Publisher

Impact Journals, LLC

Subject

Cell Biology,Aging

Cited by 3 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. Exploring the complexities of 1C metabolism: implications in aging and neurodegenerative diseases;Frontiers in Aging Neuroscience;2024-01-04

2. A case of MTHFR deficiency characterized by adult-onset spastic paraplegia;QJM: An International Journal of Medicine;2023-11-16

3. Novel compound heterozygous mutations of MTHFR Gene in a Chinese family with homocystinuria due to MTHFR deficiency;BMC Medical Genomics;2022-12-25

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