Generation and Characterization of Novel iPSC Lines from a Portuguese Family Bearing Heterozygous and Homozygous
GRN mutations
Portuguese family
frontotemporal lobar degeneration
human-induced pluripotent stem cells
reprograming
Journal
Biomedicines
ISSN: 2227-9059
Titre abrégé: Biomedicines
Pays: Switzerland
ID NLM: 101691304
Informations de publication
Date de publication:
06 Aug 2022
06 Aug 2022
Historique:
received:
06
07
2022
revised:
02
08
2022
accepted:
04
08
2022
entrez:
26
8
2022
pubmed:
27
8
2022
medline:
27
8
2022
Statut:
epublish
Résumé
Mutations in granulin (
Identifiants
pubmed: 36009452
pii: biomedicines10081905
doi: 10.3390/biomedicines10081905
pmc: PMC9405606
pii:
doi:
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : Takeda (Japan)
ID : COCKPI-T Program
Organisme : Fundação para a Ciência e Tecnologia
ID : PTDC/MEC-NEU/4814/2020
Organisme : Fundação para a Ciência e Tecnologia
ID : CENTRO-01-0145-FEDER-000008 (BrainHealth2020)
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