Genetic Metabolic Disorders Research Review Issue 5

In this issue:

Neuropsychiatric conditions in inborn errors of metabolism
Serine deficiency disorders
Disease course and complications of alpha-mannosidosis
Enzyme replacement therapy for alpha-mannosidosis
Hydroxycobalamin dose escalation in cobalamin C deficiency
Glutathione metabolism in cobalamin C deficiency
Optimising Hydroxycobalamin in cobalamin C deficiency
Adipose transplant for BCCA metabolism defects in mice
Structural design of a BCKDC inhibitor
Predicting mucopolysaccharidosis type 1 phenotype

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