HMG CoA lyase deficiency: identification of five causal point mutations in codons 41 and 42, including a frequent Saudi Arabian mutation, R41Q. (Q34384562)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | HMG CoA lyase deficiency: identification of five causal point mutations in codons 41 and 42, including a frequent Saudi Arabian mutation, R41Q. |
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HMG CoA lyase deficiency: identification of five causal point mutations in codons 41 and 42, including a frequent Saudi Arabian mutation, R41Q. (English)
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G A Mitchell
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P T Ozand
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M F Robert
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L Ashmarina
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J Roberts
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K M Gibson
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R J Wanders
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S Wang
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I Chevalier
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E Plöchl
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H Miziorko
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1 February 1998
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62
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295-300
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