Volume 2, Issue 4

Journal of Inherited Metabolic Disease is now archived and no longer receiving submissions with this publisher. All articles published in the journal during its time with Springer will remain fully searchable through our websites.

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December 1979

4 articles in this issue

Observations indicating the nature of the mutation in phenylketonuria
K. H. Choo
R. G. H. Cotton
D. M. Danks
OriginalPaper Pages: 79 - 84
Trimethylaminuria
Elizabeth Spellacy
R. W. E. Watts
S. K. Goolamali
OriginalPaper Pages: 85 - 88
α-aminoadipic aciduria: Chemical and enzymatic studies
R. G. F. Gray
E. M. O'Neill
R. J. Pollitt
OriginalPaper Pages: 89 - 92
Possible explanation for hyperglycinaemia in propionic acidaemia and methylmalonic acidaemia: Propionate and methylmalonate inhibit liver and brain mitochondrial glycine transport
M. Ugarte
J. Lopez-Lahoya
F. Valdivieso
OriginalPaper Pages: 93 - 96

Volume 2, Issue 4

Observations indicating the nature of the mutation in phenylketonuria

Trimethylaminuria

α-aminoadipic aciduria: Chemical and enzymatic studies

Possible explanation for hyperglycinaemia in propionic acidaemia and methylmalonic acidaemia: Propionate and methylmalonate inhibit liver and brain mitochondrial glycine transport

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