Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndrome (Q46695318)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndrome |
scientific article |
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Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndrome (English)
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Ching-Wan Lam
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Yuet-Ping Yuen
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Wai-Fun Cheng
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Yan-Wo Chan
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Sui-Fan Tong
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8 September 2005
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364
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1-2
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256-259
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