Oligosaccharide analysis in urine by maldi-tof mass spectrometry for the diagnosis of lysosomal storage diseases. [electronic resource]
Producer: 20131104Description: 1357-68 p. digitalISSN:- 1530-8561
- Adolescent
- Aspartylglucosaminuria -- diagnosis
- Child
- Child, Preschool
- Female
- Fucosidosis -- diagnosis
- Gangliosidoses, GM2 -- diagnosis
- Gangliosidosis, GM1 -- diagnosis
- Gaucher Disease -- diagnosis
- Glycogen Storage Disease Type II -- diagnosis
- Humans
- Infant
- Infant, Newborn
- Lysosomal Storage Diseases -- diagnosis
- Male
- Mannosidase Deficiency Diseases -- diagnosis
- Mucolipidoses -- diagnosis
- Oligosaccharides -- urine
- Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization -- methods
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Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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