This poster was presented at APHL NBSGTS 2019 in Chicago, IL by authors Tracy Klug and Heather Bilyeu, Missouri State Public Health Laboratory. Mucopolysaccharidosis Type II (MPS II), also known as Hunter syndrome, is a lysosomal storage disorder (LSD) caused by a deficiency of the lysosomal enzyme iduronate-2-sulfatase (IDS).
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