Analysis of SLC7A9 gene mutations among Jordanian patients with cystinuria

BACKGROUND: Cystinuria is known as a heritable disorder affecting the cysteine reabsorption by renal system as well as the reabsorption of dibasic amino acids. The main objectives of the present study were to identify genetic mutations in SLC7A9 gene associated with cystinuria. METHODS: A cross sect...

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Detalles Bibliográficos
Autores principales: Halalsheh, Omar M., Al-Shehabat, Mustafa A., Al-Ghazo, Moh''D.A., Al-Ghalayini, Ibrahim F., Altal, Yaman A., Al-Okour, Radwan, Altal, Omar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Cross-sectional Study
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7930589/
https://www.ncbi.nlm.nih.gov/pubmed/33680451
http://dx.doi.org/10.1016/j.amsu.2021.102182

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7930589/
https://www.ncbi.nlm.nih.gov/pubmed/33680451
http://dx.doi.org/10.1016/j.amsu.2021.102182

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