Profound neurological presentation resulting from homozygosity for a mild glutaryl-CoA dehydrogenase mutation with a minimal biochemical phenotype. (Q48249296)
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scientific article published in January 2003
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Profound neurological presentation resulting from homozygosity for a mild glutaryl-CoA dehydrogenase mutation with a minimal biochemical phenotype. |
scientific article published in January 2003 |
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Profound neurological presentation resulting from homozygosity for a mild glutaryl-CoA dehydrogenase mutation with a minimal biochemical phenotype. (English)
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E P Treacy
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A Lee-Chong
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G Roche
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B Lynch
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S Ryan
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S Goodman
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1 January 2003
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26
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1
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72-74
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