Fibrinogen Šumperk II: dysfibrinogenemia in an individual with two coding mutations. [electronic resource]
Producer: 20120619Description: 555-7 p. digitalISSN:- 1096-8652
- Adult
- Afibrinogenemia -- blood
- Blood Protein Electrophoresis
- Child
- Codon, Nonsense
- Female
- Fibrin -- ultrastructure
- Fibrinogens, Abnormal -- genetics
- Fibrinopeptide A -- metabolism
- Hemorrhagic Disorders -- etiology
- Heterozygote
- Humans
- Male
- Microscopy, Electron, Scanning
- Middle Aged
- Point Mutation
- Protein Processing, Post-Translational
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Publication Type: Case Reports; Journal Article
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