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Autor:
Anita Csorba, Gábor Katona, Mária Budai-Szűcs, Diána Balogh-Weiser, Péter Molnár, Erika Maka, Adrienn Kazsoki, Márton Vajna, Romána Zelkó, Zoltán Zsolt Nagy, György T. Balogh
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 3, p 1623 (2024)
Cystinosis is a low-prevalence lysosomal storage disease. The pathomechanism involves abnormal functioning of the cystinosine lysosomal cystine transporter (CTNS), causing intraliposomal accumulation of the amino acid cysteine disulfide, which crysta
Externí odkaz:
https://doaj.org/article/9c83360b3fc04dd2b09ffd5402eeb1d6
