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Recurrent cerebral venous thrombosis associated with heterozygote methylenetetrahydrofolate reductase C677T mutation and sickle cell trait without homocysteinemia: An autopsy case report and review of literature

✍ Scribed by Ali, Z.; Troncoso, J.C.; Fowler, D.R.


Book ID
127265200
Publisher
Elsevier Science
Year
2014
Tongue
English
Weight
501 KB
Volume
242
Category
Article
ISSN
0379-0738

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