Article
Detection of the Glanzmann's thrombasthenia mutations in Arab and Iraqi-Jewish patients by polymerase chain reaction and restriction analysis of blood or urine samples.
Thrombosis and haemostasis - 1 Oct 1991
Peretz H, Seligsohn U, Zwang E, Coller B S, Newman P J
Abstract excerpt
Severe Glanzmann's thrombasthenia is relatively frequent in Iraqi-Jews and Arabs residing in Israel. We have recently described the mutations responsible for the disease in Iraqi-Jews--an 11 base pair deletion in exon 12 of the glycoprotein IIIa gene, and in Arabs--a 13 base pair deletion at the...
Topics
- Base Sequence
- Humans
- Iraq
- Israel
- Jews
- Molecular Sequence Data
- Mutation
- Pedigree
- Polymerase Chain Reaction
- Restriction Mapping
- Thrombasthenia
