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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...

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Autors principals: Branson, Herman E., Endo, Yasuyuki, Fagin, Awilda R., Schlutz, Michael
Format: Artigo
Idioma:Inglês
Publicat: 1984
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2609761/
https://ncbi.nlm.nih.gov/pubmed/6209408
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