Hutchinson–Gilford Syndrome (Progeria) with Heterozygous Mutation in the LMNA Gene-ENST00000368300.9 Presenting with Mandibuloacral Dysplasia and Acrogeroid Features—Overlap of Premature Aging Syndromes

Detalles Bibliográficos
Autores principales: Muralidharan, Sniya, Nair, Sukumaran Pradeep, Hariharan, Sankar V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Concise Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9595151/
https://www.ncbi.nlm.nih.gov/pubmed/36304657
http://dx.doi.org/10.4103/idoj.idoj_635_21

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9595151/
https://www.ncbi.nlm.nih.gov/pubmed/36304657
http://dx.doi.org/10.4103/idoj.idoj_635_21

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