Hypoketonuric 3-hydroxydicarboxylic aciduria in five patients with glycogen storage disease

C. E. Mize; L. J. Waber; T. Anderson; M. J. Bennett

doi:10.1023/A:1005354701187

Hypoketonuric 3-hydroxydicarboxylic aciduria in five patients with glycogen storage disease

C. E. Mize, L. J. Waber, T. Anderson, M. J. Bennett

Pediatrics

Research output: Contribution to journal › Article › peer-review

4 Scopus citations

Original language	English (US)
Pages (from-to)	407-410
Number of pages	4
Journal	Journal of Inherited Metabolic Disease
Volume	20
Issue number	3
DOIs	https://doi.org/10.1023/A:1005354701187
State	Published - 1997

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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title = "Hypoketonuric 3-hydroxydicarboxylic aciduria in five patients with glycogen storage disease",

author = "Mize, {C. E.} and Waber, {L. J.} and T. Anderson and Bennett, {M. J.}",

year = "1997",

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T1 - Hypoketonuric 3-hydroxydicarboxylic aciduria in five patients with glycogen storage disease

AU - Mize, C. E.

AU - Waber, L. J.

AU - Anderson, T.

AU - Bennett, M. J.

PY - 1997

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EP - 410

JO - Journal of Inherited Metabolic Disease

JF - Journal of Inherited Metabolic Disease

IS - 3

ER -

Hypoketonuric 3-hydroxydicarboxylic aciduria in five patients with glycogen storage disease

ASJC Scopus subject areas

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