Cone Dystrophy Associated with a Novel Variant in the Terminal Codon of the


Journal

Genes
ISSN: 2073-4425
Titre abrégé: Genes (Basel)
Pays: Switzerland
ID NLM: 101551097

Informations de publication

Date de publication:
29 03 2021
Historique:
received: 23 01 2021
revised: 23 03 2021
accepted: 24 03 2021
entrez: 3 4 2021
pubmed: 4 4 2021
medline: 17 8 2021
Statut: epublish

Résumé

Mutations in

Identifiants

pubmed: 33805381
pii: genes12040499
doi: 10.3390/genes12040499
pmc: PMC8066792
pii:
doi:

Substances chimiques

Codon 0
Eye Proteins 0
RPGR protein, human 0

Types de publication

Case Reports Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Vlasta Hadalin (V)

Eye Hospital, University Medical Centre Ljubljana, Grablovičeva 46, 1000 Ljubljana, Slovenia.

Maja Šuštar (M)

Eye Hospital, University Medical Centre Ljubljana, Grablovičeva 46, 1000 Ljubljana, Slovenia.

Marija Volk (M)

Clinical Institute of Medical Genetics, University Medical Centre Ljubljana, Šlajmerjeva ulica 4, 1000 Ljubljana, Slovenia.

Aleš Maver (A)

Clinical Institute of Medical Genetics, University Medical Centre Ljubljana, Šlajmerjeva ulica 4, 1000 Ljubljana, Slovenia.

Jana Sajovic (J)

Eye Hospital, University Medical Centre Ljubljana, Grablovičeva 46, 1000 Ljubljana, Slovenia.

Martina Jarc-Vidmar (M)

Eye Hospital, University Medical Centre Ljubljana, Grablovičeva 46, 1000 Ljubljana, Slovenia.

Borut Peterlin (B)

Clinical Institute of Medical Genetics, University Medical Centre Ljubljana, Šlajmerjeva ulica 4, 1000 Ljubljana, Slovenia.

Marko Hawlina (M)

Eye Hospital, University Medical Centre Ljubljana, Grablovičeva 46, 1000 Ljubljana, Slovenia.

Ana Fakin (A)

Eye Hospital, University Medical Centre Ljubljana, Grablovičeva 46, 1000 Ljubljana, Slovenia.

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Classifications MeSH