The coding sequence of the hemolytically inactive C4A6 allotype of human complement component C4 reveals that a single arginine to tryptophan substitution at beta-chain residue 458 is the likely cause of the defect (Q31149957)
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scientific article published on May 1, 1992
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | The coding sequence of the hemolytically inactive C4A6 allotype of human complement component C4 reveals that a single arginine to tryptophan substitution at beta-chain residue 458 is the likely cause of the defect |
scientific article published on May 1, 1992 |
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The coding sequence of the hemolytically inactive C4A6 allotype of human complement component C4 reveals that a single arginine to tryptophan substitution at beta-chain residue 458 is the likely cause of the defect (English)
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Anderson MJ
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Milner CM
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Cotton RG
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Campbell RD
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1 reference