First Identification of Rare Exonic and Deep Intronic Splice-Altering Variants in Patients With Beta-Sarcoglycanopathy
BackgroundThe precise genetic diagnosis of a sarcoglycanopathy or dystrophinopathy is sometimes extremely challenging, as pathogenic non-coding variants and/or complex structural variants do exist in DMD or sarcoglycan genes. This study aimed to determine the genetic diagnosis of three patients from...
Saved in:
Main Authors: | Zhiying Xie (Author), Chengyue Sun (Author), Chang Liu (Author), Xujun Chu (Author), Qiang Gang (Author), Meng Yu (Author), Yiming Zheng (Author), Lingchao Meng (Author), Fan Li (Author), Dongliang Xia (Author), Li Wang (Author), Ying Li (Author), Jianwen Deng (Author), He Lv (Author), Zhaoxia Wang (Author), Wei Zhang (Author), Yun Yuan (Author) |
---|---|
Format: | Book |
Published: |
Frontiers Media S.A.,
2022-06-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Unraveling synonymous and deep intronic variants causing aberrant splicing in two genetically undiagnosed epilepsy families
by: Qiang Li, et al.
Published: (2021) -
Antisense Oligonucleotide Mediated Splice Correction of a Deep Intronic Mutation in OPA1
by: Tobias Bonifert, et al.
Published: (2016) -
Corrigendum to "Antisense Oligonucleotide Mediated Splice Correction of a Deep Intronic Mutation in OPA1"
Published: (2016) -
Effects of a Common Eight Base Pairs Duplication at the Exon 7-Intron 7 Junction on Splicing, Expression, and Function of OCT1
by: Sarah Römer, et al.
Published: (2021) -
Intronic position +9 and −9 are potentially splicing sites boundary from intronic variants analysis of whole exome sequencing data
by: Li Zhang, et al.
Published: (2023)