Hereditary multiple osteochondromas in Jordanian patients: Mutational and immunohistochemical analysis of EXT1 and EXT2 genes

The aim of the present study was to investigate the molecular characteristics of hereditary multiple osteochondromas (HMO) in a subset of Jordanian patients with a focus on the genetic variants of exostosin (EXT1)/(EXT2) and their protein expression. Patients with HMO and their family members were i...

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Detalles Bibliográficos
Autores principales: Mohaidat, Ziyad, Bodoor, Khaldon, Almomani, Rowida, Alorjani, Mohammed, Awwad, Mohammad-Akram, Bany-Khalaf, Audai, Al-Batayneh, Khalid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2021
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7798038/
https://www.ncbi.nlm.nih.gov/pubmed/33552269
http://dx.doi.org/10.3892/ol.2020.12412

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7798038/
https://www.ncbi.nlm.nih.gov/pubmed/33552269
http://dx.doi.org/10.3892/ol.2020.12412

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