Rapid Identification of Biallelic
Hereditary spherocytosis
Medical genomics
Rapid exome sequencing
Red cell membrane defects
Red cells
Journal
Molecular syndromology
ISSN: 1661-8769
Titre abrégé: Mol Syndromol
Pays: Switzerland
ID NLM: 101525192
Informations de publication
Date de publication:
Feb 2020
Feb 2020
Historique:
accepted:
05
12
2019
entrez:
8
4
2020
pubmed:
8
4
2020
medline:
8
4
2020
Statut:
ppublish
Résumé
Heterozygous pathogenic variants in
Identifiants
pubmed: 32256302
doi: 10.1159/000505886
pii: msy-0011-0050
pmc: PMC7109415
doi:
Types de publication
Journal Article
Langues
eng
Pagination
50-55Informations de copyright
Copyright © 2020 by S. Karger AG, Basel.
Déclaration de conflit d'intérêts
The authors have no conflicts of interest to declare.
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