Child-Onset Cerebellar Ataxia Caused by Two Compound Heterozygous Variants in ADPRS Gene: A Case Report
Background: Gene variants of ADP-ribosylserine hydrosylase, also known as ADP-ribosylhydrolase-like 2 (ADPRS or ADPRLH2; OMIM: 610624), can cause stress-induced childhood-onset neurodegeneration with variable ataxia and seizures (CONDSIAS, OMIM: 618170), an ultra-rare neurodegenerative autosomal rec...
Main Authors: | Jiehui Ma, Qiaoqiao Qian, Shuang Yan, Haoyu Dou, Cheng Li, Dan Sun |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2022-05-01
|
Series: | Frontiers in Genetics |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fgene.2021.788702/full |
Similar Items
-
Nonsense-mediated decay machinery in Plasmodium falciparum is inefficient and non-essential
by: Emma McHugh, et al.
Published: (2023-08-01) -
MicroRNA-mediated repression of nonsense mRNAs
by: Ya Zhao, et al.
Published: (2014-08-01) -
A nonsense variant in FBN1 caused autosomal dominant Marfan syndrome in a Chinese family: a case report
by: Yuping Niu, et al.
Published: (2020-10-01) -
Concise Syntheses of Trifluoromethylated Cyclic and Acyclic Analogues of cADPR
by: Lihe Zhang, et al.
Published: (2010-11-01) -
2′-deoxy-ADPR activates human TRPM2 faster than ADPR and thereby induces higher currents at physiological Ca2+ concentrations
by: Jelena Pick, et al.
Published: (2024-01-01)