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MYRF: A Mysterious Membrane-Bound Transcription Factor Involved in Myelin Development and Human Diseases.

作者信息

Huang Hao, Zhou Fang, Zhou Shiyou, Qiu Mengsheng

机构信息

Institute of Life Sciences, Zhejiang Key Laboratory of Organ Development and Regeneration, College of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou, 311121, China.

The State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center at Sun Yat-sen University, Guangzhou, 510060, China.

出版信息

Neurosci Bull. 2021 Jun;37(6):881-884. doi: 10.1007/s12264-021-00678-9. Epub 2021 Apr 17.

DOI:10.1007/s12264-021-00678-9
PMID:33864620
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8192642/
Abstract
摘要

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本文引用的文献

1
Autosomal dominant nanophthalmos and high hyperopia associated with a C-terminal frameshift variant in .常染色体显性小眼球症和高度远视与……中的一个C末端移码变异相关
Mol Vis. 2019 Sep 21;25:527-534. eCollection 2019.
2
Review of the phenotypic spectrum associated with haploinsufficiency of MYRF.MYRF 部分单体型不足相关表型谱的综述
Am J Med Genet A. 2019 Jul;179(7):1376-1382. doi: 10.1002/ajmg.a.61182. Epub 2019 May 8.
3
Novel TMEM98 mutations in pedigrees with autosomal dominant nanophthalmos.常染色体显性小眼球家族中的新型跨膜蛋白98（TMEM98）突变。
Mol Vis. 2015 Sep 1;21:1017-23. eCollection 2015.