Rapid screening of copy number variations in
Genetics research
Neurodegenerative diseases
Journal
Human genome variation
ISSN: 2054-345X
Titre abrégé: Hum Genome Var
Pays: England
ID NLM: 101652445
Informations de publication
Date de publication:
2019
2019
Historique:
received:
13
04
2019
revised:
31
07
2019
accepted:
01
08
2019
entrez:
25
10
2019
pubmed:
28
10
2019
medline:
28
10
2019
Statut:
epublish
Résumé
Copy number variations (CNVs) are commonly reported in
Identifiants
pubmed: 31645979
doi: 10.1038/s41439-019-0075-5
pii: 75
pmc: PMC6804619
doi:
Types de publication
Journal Article
Langues
eng
Pagination
41Informations de copyright
© The Author(s) 2019.
Déclaration de conflit d'intérêts
Conflict of interestThe authors declare that they have no conflict of interest.
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