Hematopoietic Disorders, Renal Impairment and Growth in Mucopolysaccharidosis-Plus Syndrome

Mucopolysaccharidoses (MPS) are rare lysosomal storage disorders (LSD) characterized by the excessive accumulation of glycosaminoglycans (GAG). Conventional MPS, caused by inborn deficiencies of lysosomal enzymes involved in GAG degradation, display various multisystemic symptoms—including progressi...

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Detalles Bibliográficos
Autores principales: Sofronova, Viktoriia, Iwata, Rina, Moriya, Takuya, Loskutova, Kiunniai, Gurinova, Elizaveta, Chernova, Mairanush, Timofeeva, Anastasia, Shvedova, Anna, Vasilev, Filipp, Novgorodova, Saina, Terawaki, Seigo, Moriwaki, Takahito, Sukhomyasova, Aitalina, Maksimova, Nadezhda, Otomo, Takanobu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9145135/
https://www.ncbi.nlm.nih.gov/pubmed/35628659
http://dx.doi.org/10.3390/ijms23105851

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9145135/
https://www.ncbi.nlm.nih.gov/pubmed/35628659
http://dx.doi.org/10.3390/ijms23105851

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