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Characterization Of Mesenchymal Stem Cells In Mucolipidosis Type Ii (I-Cell Disease)
KÖSE, Sevil; AERTS KAYA, Fatima; KUŞKONMAZ, Barış; UÇKAN ÇETİNKAYA, Duygu (2019)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 ...