Multiplexing Iduronate-2-Sulphatase (MPS-II) into a 7-Plex Lysosomal Storage Disorder MS/MS Assay Using Cold-Induced Phase Separation

Mucopolysaccharidosis type II (MPS-II, Hunter syndrome, OMIM:30990) is a lysosomal storage disorder (LSD) that results in iduronate 2-sulphatase (I2S) enzyme deficiency. MPS-II was added to the Recommended Uniform Screening Panel (RUSP) in August 2022; thus, there is an increased demand for multiple...

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Detalles Bibliográficos
Autores principales: Courtney, Elya, Pickens, C. Austin, Cuthbert, Carla, Petritis, Konstantinos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Technical Note
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10298912/
https://www.ncbi.nlm.nih.gov/pubmed/37367213
http://dx.doi.org/10.3390/ijns9020032

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10298912/
https://www.ncbi.nlm.nih.gov/pubmed/37367213
http://dx.doi.org/10.3390/ijns9020032

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