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Links from PubMed

Items: 3

1.

Impaired cotranslational processing as a mechanism for type I antithrombin deficiency.

Fitches AC, Appleby R, Lane DA, De Stefano V, Leone G, Olds RJ.

Blood. 1998 Dec 15;92(12):4671-6.

2.
3.

The molecular genetics of antithrombin deficiency.

Olds RJ, Lane DA, Thein SL.

Br J Haematol. 1994 Jun;87(2):221-6. Review. No abstract available.

PMID:
7947262

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