Pseudohemophilia of Erik von Willebrand caused by homozygous one nucleotide deletion in exon 18 of t

• 作 者: Alain Gadisseur Zwi Berneman W
• 机 构: Hemostasis,DepartmentofHematology,GoodheartInstituteandFoundation
• 出 处: 世界血液学杂志
• 发表日期: 2013年4期
• 关键词: Autosomal RECESSIVE von Willebrand DISEASE type 3 and 1 Molecular etiology Carri

The original description of a novel severe bleeding disorder as“Hereditary Pseudohemophilia”by Erik von Willebrand can currently be labelled as von Willebrand disease(VWD)type 3.VWD type 3 is autosomal recessive caused by homozygous or double heterozygous