Status of newborn screening and follow up investigations for Mucopolysaccharidoses I and II in Taiwan

BACKGROUND: Mucopolysaccharidoses (MPS) are lysosomal storage diseases in which mutations of genes encoding for lysosomal enzymes cause defects in the degradation of glycosaminoglycans (GAGs). The accumulation of GAGs in lysosomes results in cellular dysfunction and clinical abnormalities. The early...

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Detalles Bibliográficos
Autores principales: Chuang, Chih-Kuang, Lin, Hsiang-Yu, Wang, Tuan-Jen, Huang, You-Hsin, Chan, Min-Ju, Liao, Hsuan-Chieh, Lo, Yun-Ting, Wang, Li-Yun, Tu, Ru-Yi, Fang, Yi-Ya, Chen, Tzu-Lin, Ho, Hui-Chen, Chiang, Chuan-Chi, Lin, Shuan-Pei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5970538/
https://www.ncbi.nlm.nih.gov/pubmed/29801497
http://dx.doi.org/10.1186/s13023-018-0816-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5970538/
https://www.ncbi.nlm.nih.gov/pubmed/29801497
http://dx.doi.org/10.1186/s13023-018-0816-4

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