Genetic Metabolic Disorders Research Review Issue 3

In this issue:

Intracellular localisation of vitamin B12 metabolism
Limitations observed in SNP array results
EPI-743 treatment of Leigh syndrome
Monitoring mitochondrial disease responses to EPI-743
Fumarylacetoacetate involved in tyrosinaemia type I
Maternal PKU: phenylalaninemia and IUGR
Lysine and renal tubular cell apoptosis
Haematopoietic stem cells effective in MPS II
Arginine + sodium phenylbutyrate for argininosuccinic aciduria
MPS IV: brain MRI findings and IQ
Bezafibrate in X-linked adrenoleukodystrophy

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