Simplified Newborn Screening Protocol for Lysosomal Storage Disorders
Simplified Newborn Screening Protocol for Lysosomal Storage Disorders
About this item
Full title
Author / Creator
Publisher
Washington, DC: American Association for Clinical Chemistry
Journal title
Language
English
Formats
Publication information
Publisher
Washington, DC: American Association for Clinical Chemistry
Subjects
More information
Scope and Contents
Contents
Interest in lysosomal storage disorders, a collection of more than 40 inherited metabolic disorders, has increased because of new therapy options such as enzyme replacement, stem cell transplantation, and substrate reduction therapy. We developed a high-throughput protocol that simplifies analytical challenges such as complex sample preparation and...
Alternative Titles
Full title
Simplified Newborn Screening Protocol for Lysosomal Storage Disorders
Authors, Artists and Contributors
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_proquest_miscellaneous_885911041
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_885911041
Other Identifiers
ISSN
0009-9147
E-ISSN
1530-8561
DOI
10.1373/clinchem.2011.164640
