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

6533b855fe1ef96bd12b1a97

RESEARCH PRODUCT

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

P. Lohse Jochen Hardt Günther Witzke Konrad Bork Karin Wulff

subject

Genetics biology business.industry Sequence analysis Intron Hematology General Medicine Coagulation Factor XII medicine.disease Phenotype Molecular biology C1-inhibitor Exon Hereditary angioedema biology.protein Medicine business Gene Genetics (clinical)

year	journal	country	edition	language
2014-08-12	Haemophilia

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

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