Molecular analysis of the AGXT gene in Syrian patients suspected with primary hyperoxaluria type 1

BACKGROUND: Characterization of the molecular basis of primary hyperoxaluria type 1 (PH-1) in Syria has been accomplished through the analysis of 90 unrelated chromosomes from 45 Syrians patients with PH-1 from different regions. METHODS: Alanine glyoxylate aminotransferase (AGXT) gene mutations hav...

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Detalles Bibliográficos
Autores principales: Murad, Hossam, Alhalabi, Mohamad Baseel, Dabboul, Amir, Alfakseh, Nour, Nweder, Mohamad Sayah, Zghib, Youssef, Wannous, Hala
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8176596/
https://www.ncbi.nlm.nih.gov/pubmed/34082749
http://dx.doi.org/10.1186/s12920-021-00996-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8176596/
https://www.ncbi.nlm.nih.gov/pubmed/34082749
http://dx.doi.org/10.1186/s12920-021-00996-x

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