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Leigh-Like Syndrome Due to Homoplasmic m.8993T>G Variant with Hypocitrullinemia and Unusual Biochemical Features Suggestive of Multiple Carboxylase Deficiency (MCD). [electronic resource] by
- Balasubramaniam, Shanti
- Lewis, B
- Mock, D M
- Said, H M
- Tarailo-Graovac, M
- Mattman, A
- van Karnebeek, C D
- Thorburn, D R
- Rodenburg, R J
- Christodoulou, J
Publication details: JIMD reports 2017
In:
JIMD reports vol. 33
Availability: No items available.
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92.
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Erratum: Leigh-Like Syndrome Due to Homoplasmic m.8993T>G Variant with Hypocitrullinemia and Unusual Biochemical Features Suggestive of Multiple Carboxylase Deficiency (MCD). [electronic resource] by
- Balasubramaniam, Shanti
- Lewis, B
- Mock, D M
- Said, H M
- Tarailo-Graovac, M
- Mattman, A
- van Karnebeek, C D
- Thorburn, D R
- Rodenburg, R J
- Christodoulou, J
Publication details: JIMD reports 2017
In:
JIMD reports vol. 33
Availability: No items available.
|