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Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase Deficiency: Unique Presenting Laboratory Values and a Review of Biochemical and Clinical Features. [electronic resource] by
- Conboy, Erin
- Vairo, Filippo
- Schultz, Matthew
- Agre, Katherine
- Ridsdale, Ross
- Deyle, David
- Oglesbee, Devin
- Gavrilov, Dimitar
- Klee, Eric W
- Lanpher, Brendan
Publication details: JIMD reports 2018
In:
JIMD reports vol. 40
Availability: No items available.
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