Variability of clinical manifestation of factor VII-deficiency in homozygous and heterozygous subjects of the European F7 gene mutation A294V
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Overview
status
publication date
- August 1, 2008
has subject area
- Amino Acid Substitution (MeSH)
- Blood Coagulation Disorders, Inherited (MeSH)
- Factor V (MeSH)
- Factor VII (MeSH)
- Factor VII Deficiency (MeSH)
- Genetic Carrier Screening (MeSH)
- Homozygote (MeSH)
- Humans (MeSH)
- Immunology (Science Metrix)
- Mutation (MeSH)
published in
- Hematology Journal Journal