Potential Benefits of Allogeneic Haploidentical Adipose Tissue-Derived Stromal Vascular Fraction in a Hutchinson–Gilford Progeria Syndrome Patient

Hutchinson–Gilford progeria syndrome (HGPS) is a rare, fatal, and genetic disorder in the LMNA gene encoding for prelamin A. Normally, prelamin A is processed to become lamin A protein. In HGPS patients, there is a heterozygous mutation in LMNA gene, in which there is a deletion of genetic codes res...

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Detalles Bibliográficos
Autores principales: Pak, Jaewoo, Lee, Jung Hun, Jeon, Jeong Ho, Kim, Young Bae, Jeong, Byeong Chul, Lee, Sang Hee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Bioengineering and Biotechnology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7643450/
https://www.ncbi.nlm.nih.gov/pubmed/33195136
http://dx.doi.org/10.3389/fbioe.2020.574010

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7643450/
https://www.ncbi.nlm.nih.gov/pubmed/33195136
http://dx.doi.org/10.3389/fbioe.2020.574010

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