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Heritable α2-Macroglobulin Deficiency in a Patient With Arterial Thrombosis: α2-Macroglobulin Deficiency Irvine
A heritable deficiency in α(2)-macroglobulin (α(2)M) was identified in a 61-year-old man with arterial thrombosis. Plasma α(2)M levels among the patient's symptom-free relatives consistently ranged from 43 to 55 percent of laboratory mean-normal values. The new α(2)M variant displayed retarded...
שמור ב:
| Main Authors: | , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
1984
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2609761/ https://ncbi.nlm.nih.gov/pubmed/6209408 |
| תגים: |
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