Work

Hemoglobin Blocks Von Willebrand Factor Proteolysis by ADAMTS-13: A Mechanism Associated with Acquired ADAMTS-13 Deficiency in Patients with Sickle Cell Disease

Year: 2008
Type: article
Source: Blood
Language: English
Subfield: Genetics
Field: Medicine
Open Access status: closed
OpenAlex ID: W2980850075
FWCI:
Cites:
Cited by: 1
Related to: 10