Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family
Published inBlood, vol. 101, no. 9, p. 3492-3494
Publication date2003
Abstract
Keywords
- Abortion, Spontaneous
- Afibrinogenemia/ diagnosis/embryology/genetics
- Amino Acid Sequence
- Amniocentesis
- Arabs/ genetics
- Codon/genetics
- Codon, Nonsense
- Consanguinity
- DNA, Complementary/genetics
- Female
- Fetal Diseases/ diagnosis/genetics
- Fibrinogen/chemistry/ genetics
- Genes, Recessive
- Genetic Predisposition to Disease
- Hemorrhagic Disorders/genetics
- Humans
- Infant, Newborn
- Male
- Molecular Sequence Data
- Pedigree
Affiliation
Citation (ISO format)
NEERMAN ARBEZ, Marguerite et al. Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family. In: Blood, 2003, vol. 101, n° 9, p. 3492–3494. doi: 10.1182/blood-2002-10-3116
Main files (1)
Article
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Identifiers
- PID : unige:8937
- DOI : 10.1182/blood-2002-10-3116
- PMID : 12511408
ISSN of the journal0006-4971