Newborn screening for lysosomal storage disorders. [electronic resource]
Producer: 20110525Description: 63-71 p. digitalISSN:- 1552-4876
- Enzyme Replacement Therapy
- Fabry Disease -- diagnosis
- Gaucher Disease -- diagnosis
- Genetic Therapy
- Glycogen Storage Disease Type II -- diagnosis
- Hematopoietic Stem Cell Transplantation
- Humans
- Hydrolases -- genetics
- Infant, Newborn
- Leukodystrophy, Globoid Cell -- diagnosis
- Lysosomal Storage Diseases -- diagnosis
- Mucopolysaccharidoses -- diagnosis
- Neonatal Screening
- Niemann-Pick Diseases -- diagnosis
- Tandem Mass Spectrometry
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review
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