A novel UBE2A mutation in a Chinese family with X‐linked intellectual disability-Reference-Cited by-同舟云学术

A novel UBE2A mutation in a Chinese family with X‐linked intellectual disability

Published:2020-04-22 Issue:8 Volume:22 Page:
ISSN:1099-498X
Container-title:The Journal of Gene Medicine
language:en
Short-container-title:J Gene Med

Author:

Jia Weimin¹,Hu Qi²,Wu Yanling¹,Wang Jiarui¹,Liu Zhenxing¹,Zhang Xianqin¹^ORCID

Affiliation:

1. Key Laboratory of Molecular Biophysics of the Ministry of Education, College of Life Science and Technology and Center for Human Genome ResearchHuazhong University of Science and Technology Wuhan Hubei China

2. Department of Geriatrics, Tongji Hospital, Tongji Medical CollegeHuazhong University of Science and Technology Wuhan Hubei China

Funder

Innovative Research Group Project of the National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics (clinical),Drug Discovery,Genetics,Molecular Biology,Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jgm.3191

Reference22 articles.

1. X-linked intellectual disability type Nascimento is a clinically distinct, probably underdiagnosed entity

2. Intracellular Protein Degradation From a Vague Idea through the Lysosome and the Ubiquitin-Proteasome System and on to Human Diseases and Drug Targeting: Nobel Lecture, December 8, 2004

3. An essential role for UBE2A/HR6A in learning and memory and mGLUR-dependent long-term depression

4. UBE2A, Which Encodes a Ubiquitin-Conjugating Enzyme, Is Mutated in a Novel X-Linked Mental Retardation Syndrome

5. SOAP2: an improved ultrafast tool for short read alignment

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