Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: clinical course and description of causal mutations in two patients (Q55670918)

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Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: clinical course and description of causal mutations in two patients
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    Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: clinical course and description of causal mutations in two patients (English)
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    L Bouchard
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    M F Robert
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    D Vinarov
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    C A Stanley
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    G N Thompson
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    A Morris
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    J V Leonard
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    P Quant
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    B Y Hsu
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    A Boneh
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    Y Boukaftane
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    L Ashmarina
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    S Wang
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    H Miziorko
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    G A Mitchell
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    March 2001
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    49
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    326-31
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    3
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