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- Adrenal Insufficiency
- Amino Acid Sequence
- Antiporters
- Child, Preschool
- Diagnosis, Differential
- Female
- Genetic Diseases, X-Linked
- Glycerol
- Glycerol Kinase
- Glycogen Storage Disease Type I
- Humans
- Infant
- Male
- Molecular Sequence Data
- Monosaccharide Transport Proteins
- Mutation
- Protein Conformation
- Pyruvate Dehydrogenase (Lipoamide)
- Pyruvate Dehydrogenase Complex Deficiency Disease
- genetics
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