Molecular characterization of properdin deficiency type III: dysfunction produced by a single point mutation in exon 9 of the structural gene causing a tyrosine to aspartic acid interchange. (Q48059014)
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scientific article published in October 1996
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Molecular characterization of properdin deficiency type III: dysfunction produced by a single point mutation in exon 9 of the structural gene causing a tyrosine to aspartic acid interchange. |
scientific article published in October 1996 |
Statements
Molecular characterization of properdin deficiency type III: dysfunction produced by a single point mutation in exon 9 of the structural gene causing a tyrosine to aspartic acid interchange (English)
Fredrikson GN
Westberg J
Kuijper EJ
Tijssen CC
Sjöholm AG
Uhlén M
1 October 1996