Ara
Toplam kayıt 1, listelenen: 1-1
Characterization Of Mesenchymal Stem Cells In Mucolipidosis Type Ii (I-Cell Disease)
(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 ...