A nonstop mutation in the factor (F)X gene of a severely haemorrhagic patient with complete absence of coagulation FX. [electronic resource]
Producer: 20080226Description: 1165-9 p. digitalISSN:- 0340-6245
- 3' Flanking Region
- Adolescent
- Base Sequence
- Blood Coagulation
- Codon, Terminator
- DNA Mutational Analysis
- Exons
- Factor X -- analysis
- Factor X Deficiency -- blood
- Genetic Predisposition to Disease
- Hemorrhage -- blood
- Homozygote
- Humans
- Male
- Molecular Sequence Data
- Mutation
- Pedigree
- Phenotype
- Polymerase Chain Reaction
- RNA Stability
- RNA, Messenger -- blood
- Severity of Illness Index
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Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural
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