Genetic Variants in the 3'UTR of
3’UTR region
BRCA1
BRCA2
hereditary breast and ovarian cancer
miRNA
polymorphism
Journal
Diagnostics (Basel, Switzerland)
ISSN: 2075-4418
Titre abrégé: Diagnostics (Basel)
Pays: Switzerland
ID NLM: 101658402
Informations de publication
Date de publication:
13 May 2020
13 May 2020
Historique:
received:
26
02
2020
revised:
01
04
2020
accepted:
10
04
2020
entrez:
17
5
2020
pubmed:
18
5
2020
medline:
18
5
2020
Statut:
epublish
Résumé
Hereditary breast and ovarian cancer (HBOC) syndrome is mainly caused by mutations in the
Identifiants
pubmed: 32414209
pii: diagnostics10050298
doi: 10.3390/diagnostics10050298
pmc: PMC7277914
pii:
doi:
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : Universidad Autonoma de Nuevo Leon
ID : Institutional Calls, PAICyT
Organisme : Consejo Nacional de Ciencia y Tecnología (CONACYT)
ID : Posgrade scholarship: 387437
Déclaration de conflit d'intérêts
The authors declare no conflict of interest.
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