Abnormal bleeding phenotype for mild haemophilia B patients with the p.Ile112Thr variation on the gene for factor IX
Haemophilia
.
2021 Jul;27(4):e462-e465.
doi: 10.1111/hae.14146.
Epub 2020 Sep 30.
Authors
Céline Row
1
,
Pierre Chamouni
2
,
Claire Berger
3
,
Anne Lienhart
4
,
Sandrine Meunier
4
,
Mathilde Fretigny
5
,
Vincent Dalibard
6
7
,
Marie Viprey
7
8
,
Hervé Chambost
9
,
Virginie Barbay
2
,
Julien Bovet
1
Affiliations
1
Thrombosis and Hemostasis Unit, University Hospital of Dijon, Dijon, France.
2
Hemophilia Treatment Center, University Hospital of Rouen, Rouen, France.
3
Hemophilia Treatment Center, Pediatric Hematology department, University Hospital of Saint Etienne, Saint Etienne, France.
4
Hospices Civils de Lyon, French Reference Centre for Hemophilia, University Hospital of Lyon, France.
5
Hemostasis Laboratory, University Hospital of Lyon, Lyon, France.
6
Lille CHRU, Hemophilia Treatment Center, Hematology and Transfusion, Lille, France.
7
APHM, FranceCoag, Research Department, Marseille, France.
8
Aix-Marseille Univ, EA 3279 CEReSS-Health Service Research and Quality of Life Center, Marseille, France.
9
APHM, Hemophilia Treatment Center, La Timone Hospital and Aix Marseille Univ, INSERM, INRA, C2VN, Marseille, France.
PMID:
32996663
DOI:
10.1111/hae.14146
No abstract available
Publication types
Letter
MeSH terms
Factor IX / genetics
Factor VIII / genetics
Hemophilia A*
Hemophilia B* / genetics
Humans
Phenotype
Substances
Factor VIII
Factor IX