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Characterization of mesenchymal stem cells in mucolipidosis type II (I-cell disease)

Mucolipidosis type II (ML-II, I-cell disease) is a fatal inherited lysosomal storage disease caused by a deficiency of the enzyme N-acetylglucosamine-1-phosphotransferase. A characteristic skeletal phenotype is one of the many clinical manifestations of ML-II. Since the mechanisms underlying these s...

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Detalles Bibliográficos
Autores principales:	KÖSE, Sevil, AERTS KAYA, Fatima, KUŞKONMAZ, Barış, UÇKAN ÇETİNKAYA, Duygu
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Scientific and Technological Research Council of Turkey 2019
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6620033/ https://www.ncbi.nlm.nih.gov/pubmed/31320815 http://dx.doi.org/10.3906/biy-1902-20

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