Validation and Implementation of a Highly Sensitive and Efficient Newborn Screening Assay for Mucopolysaccharidosis Type II

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). MPS II satisfies all criteria defined by the Advisory Committee on Heritable Disorders in Newborns and Children (AC...

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Bibliographic Details
Main Authors: Heather Bilyeu (Author), Jon Washburn (Author), Lacey Vermette (Author), Tracy Klug (Author)
Format: Book
Published: MDPI AG, 2020-10-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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