Hutchinson-Gilford Progeria Syndrome: Clinical and Molecular Characterization.
HGPS
genetic assessment
laminopathy
premature aging
progeria
treatment
Journal
The application of clinical genetics
ISSN: 1178-704X
Titre abrégé: Appl Clin Genet
Pays: New Zealand
ID NLM: 101579789
Informations de publication
Date de publication:
2020
2020
Historique:
received:
15
11
2019
accepted:
13
05
2020
entrez:
18
9
2020
pubmed:
19
9
2020
medline:
19
9
2020
Statut:
epublish
Résumé
Hutchinson-Gilford progeria syndrome (HGPS) is a rare congenital disease caused by mutations in the
Identifiants
pubmed: 32943904
doi: 10.2147/TACG.S238715
pii: 238715
pmc: PMC7481268
doi:
Types de publication
Case Reports
Langues
eng
Pagination
159-164Informations de copyright
© 2020 Pachajoa et al.
Déclaration de conflit d'intérêts
The authors report no conflicts of interest in this work.
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