WGS and RNA Studies Diagnose Noncoding
Journal
Neurology. Genetics
ISSN: 2376-7839
Titre abrégé: Neurol Genet
Pays: United States
ID NLM: 101671068
Informations de publication
Date de publication:
Feb 2021
Feb 2021
Historique:
received:
01
05
2020
accepted:
19
11
2020
entrez:
12
5
2021
pubmed:
13
5
2021
medline:
13
5
2021
Statut:
epublish
Résumé
To describe the diagnostic utility of whole-genome sequencing and RNA studies in boys with suspected dystrophinopathy, for whom multiplex ligation-dependent probe amplification and exomic parallel sequencing failed to yield a genetic diagnosis, and to use remnant normal Exome, genome, and/or muscle RNA sequencing was performed for 7 males with elevated creatine kinase. PCR of muscle-derived complementary DNA (cDNA) studied consequences for Splice-altering intronic single nucleotide variants or structural rearrangements in Whole-genome sequencing relied heavily on RNA studies to identify
Identifiants
pubmed: 33977140
doi: 10.1212/NXG.0000000000000554
pii: NG2020014225
pmc: PMC8105888
doi:
Types de publication
Journal Article
Comment
Langues
eng
Pagination
e554Subventions
Organisme : NCATS NIH HHS
ID : UL1 TR001863
Pays : United States
Commentaires et corrections
Type : CommentOn
Informations de copyright
Copyright © 2021 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology.
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