A distinct common p.Gln317* mutation among causative LMAN1 genetic mutations of combined factor V and factor VIII deficiency in five Taiwanese families.

Subjects

Subjects :

Factor V genetics
Factor VIII genetics
Humans
Mutation
Factor V Deficiency genetics
Hemophilia A genetics
Mannose-Binding Lectins genetics
Membrane Proteins genetics

Details

Language :

English

ISSN :

1365-2516

Volume :

28

Issue :

1

Database :

MEDLINE

Journal :

Haemophilia : the official journal of the World Federation of Hemophilia

Publication Type :

Editorial & Opinion

Accession number :

34766420

Full Text :

https://doi.org/10.1111/hae.14458