Metabolomic Analyses to Identify Candidate Biomarkers of Cystinosis

Cystinosis is a rare, devastating hereditary disease secondary to recessive CTNS gene mutations. The most commonly used diagnostic method is confirmation of an elevated leukocyte cystine level; however, this method is expensive and difficult to perform. This study aimed to identify candidate biomark...

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Detalles Bibliográficos
Autores principales: Nemutlu, Emirhan, Ozaltin, Fatih, Yabanoglu-Ciftci, Samiye, Gulhan, Bora, Eylem, Cemil Can, Baysal, İpek, Gök-Topak, Elif Damla, Ulubayram, Kezban, Sezerman, Osman Ugur, Ucar, Gulberk, Kır, Sedef, Topaloglu, Rezan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9916752/
https://www.ncbi.nlm.nih.gov/pubmed/36768921
http://dx.doi.org/10.3390/ijms24032603

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9916752/
https://www.ncbi.nlm.nih.gov/pubmed/36768921
http://dx.doi.org/10.3390/ijms24032603

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