Determinants of Disease Penetrance in
CNOT3
MSR1
PRPF31
RP11
induced pluripotent stem cells
non-penetrance
retinal organoid
retinal pigment epithelium
retinitis pigmentosa
rod-cone dystrophy
Journal
Genes
ISSN: 2073-4425
Titre abrégé: Genes (Basel)
Pays: Switzerland
ID NLM: 101551097
Informations de publication
Date de publication:
28 09 2021
28 09 2021
Historique:
received:
04
09
2021
revised:
25
09
2021
accepted:
27
09
2021
entrez:
23
10
2021
pubmed:
24
10
2021
medline:
9
2
2022
Statut:
epublish
Résumé
Retinitis pigmentosa 11 (RP11) is caused by dominant mutations in
Identifiants
pubmed: 34680937
pii: genes12101542
doi: 10.3390/genes12101542
pmc: PMC8535263
pii:
doi:
Substances chimiques
CNOT3 protein, human
0
Eye Proteins
0
MSR1 protein, human
0
PRPF31 protein, human
0
Scavenger Receptors, Class A
0
Transcription Factors
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
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