A founder deletion in the
Disease genetics
Rare variants
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:
21
05
2019
revised:
08
08
2019
accepted:
09
08
2019
entrez:
25
10
2019
pubmed:
28
10
2019
medline:
28
10
2019
Statut:
epublish
Résumé
Congenital stationary night blindness (CSNB) is a disease affecting the night vision of individuals. Previous studies identified
Identifiants
pubmed: 31645983
doi: 10.1038/s41439-019-0076-4
pii: 76
pmc: PMC6804618
doi:
Types de publication
Journal Article
Langues
eng
Pagination
45Informations de copyright
© The Author(s) 2019.
Déclaration de conflit d'intérêts
Conflict of interestM.P. is an employee of PreventionGenetics, an accredited clinical DNA testing laboratory. C.J.P. is Director of the Molecular Vision Laboratory. The remaining authors declare no conflict of interest.
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