Codi QR

Unprecedented report: First female monozygotic twins as carriers of Hutchinson-Gilford progeria syndrome

Hutchinson-Gilford Progeria Syndrome (HGPS) is a rare genetic condition characterized by premature aging resulting from an autosomal mutation in the LMNA gene. This article presents a groundbreaking instance of the first female monozygotic twins affected by HGPS, originating from Brazil, highlighti...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: Nelson Carlos Reis-Filho, Thays Karolyne Ponte Prado Aguiar, Dafnin Lima Souza Ramos, Bruna Mariah Martins Müller, Isadora Sousa Oliveira, Felipe Augusto Cerni, Manuela Berto Pucca
Format: Artigo
Idioma:Inglês
Publicat: Aydın Pediatric Society 2024-06-01
Col·lecció:Trends in Pediatrics
Matèries:
Accés en línia:https://trendspediatrics.com/article/view/115
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!