A Common 3'UTR Variant of the
PHOX2B
gene expression regulation
idiopathic apparent life threatening event
miR-204
sudden infant death syndrome
sudden unexpected infant death
Journal
Frontiers in neurology
ISSN: 1664-2295
Titre abrégé: Front Neurol
Pays: Switzerland
ID NLM: 101546899
Informations de publication
Date de publication:
2021
2021
Historique:
received:
16
12
2020
accepted:
02
02
2021
entrez:
5
4
2021
pubmed:
6
4
2021
medline:
6
4
2021
Statut:
epublish
Résumé
Heterozygous mutations in the Paired like homeobox 2b (
Identifiants
pubmed: 33815256
doi: 10.3389/fneur.2021.642735
pmc: PMC8017182
doi:
Types de publication
Journal Article
Langues
eng
Pagination
642735Informations de copyright
Copyright © 2021 Bachetti, Bagnasco, Piumelli, Palmieri and Ceccherini.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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