Complementation cloning identifies CDG-IIc, a new type of congenital disorders of glycosylation, as a GDP-fucose transporter deficiency. [electronic resource]
Producer: 20010531Description: 73-6 p. digitalISSN:- 1061-4036
- Amino Acid Sequence
- Biological Transport
- Carrier Proteins -- genetics
- Cells, Cultured
- Cloning, Molecular
- Congenital Disorders of Glycosylation -- classification
- Fibroblasts -- cytology
- Genetic Complementation Test
- Glycosylation
- Guanosine Diphosphate Fucose -- metabolism
- Humans
- Male
- Molecular Sequence Data
- Monosaccharide Transport Proteins
- Sequence Homology, Amino Acid
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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