Characterization of a partial exon 9/intron 9 deletion in the coagulation factor XII gene (F12) detected in two Turkish families with hereditary angioedema and normal C1 inhibitor.

Subjects

Subjects :

Adult
Angioedemas, Hereditary metabolism
Asian People genetics
Exons
Factor XII metabolism
Female
Humans
Introns
Male
Middle Aged
Phenotype
Sequence Analysis, DNA
Turkey
Young Adult
Angioedemas, Hereditary genetics
Complement C1 Inhibitor Protein metabolism
Factor XII genetics
Sequence Deletion

Details

Language :

English

ISSN :

1365-2516

Volume :

20

Issue :

5

Database :

MEDLINE

Journal :

Haemophilia : the official journal of the World Federation of Hemophilia

Publication Type :

Report

Accession number :

25113305

Full Text :

https://doi.org/10.1111/hae.12519