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1.
Antithrombin deficiency in three Japanese families: one novel and two reported point mutations in the antithrombin gene.
Thromb Res
; 132(2): e118-23, 2013 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-23809926
2.
Two case reports of inherited antithrombin deficiency: a novel frameshift mutation and a large deletion including all seven exons detected using two methods.
Int J Hematol
; 93(2): 216-219, 2011 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-21240680
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