2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency: an X-linked inborn error of isoleucine metabolism that may mimic a mitochondrial disease (Q46691234)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency: an X-linked inborn error of isoleucine metabolism that may mimic a mitochondrial disease |
scientific article |
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2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency: an X-linked inborn error of isoleucine metabolism that may mimic a mitochondrial disease (English)
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Ronald J A Wanders
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Celia Perez-Cerda
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Judit García-Villoria
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Rob Ofman
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Pedro Ruiz Sala
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Begoña Merinero
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Julio Ramos
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Maria Teresa García-Silva
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Beatriz Beseler
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Jaime Dalmau
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Magdalena Ugarte
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Antonia Ribes
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1 September 2005
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58
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3
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488-491
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