Origin and timing of de novo variants implicated in type 2 von Willebrand disease.

Chen, Ming; Shen, Ming-Ching; Chang, Shun-Ping; Ma, Gwo-Chin; Huang, Ying-Chih; Lin, Ching-Yeh

Chen, Ming; Shen, Ming-Ching; Chang, Shun-Ping; Ma, Gwo-Chin; Huang, Ying-Chih; Lin, Ching-Yeh.

Afiliação

Chen M; Department of Genomic Medicine, Changhua Christian Hospital, Changhua, Taiwan.
Shen MC; Department of Obstetrics and Gynecology, National Taiwan University Hospital, Taipei, Taiwan.
Chang SP; Department of Internal Medicine, Changhua Christian Hospital, Changhua, Taiwan.
Ma GC; Department of Laboratory Medicine and Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Huang YC; Department of Genomic Medicine, Changhua Christian Hospital, Changhua, Taiwan.
Lin CY; Department of Genomic Medicine, Changhua Christian Hospital, Changhua, Taiwan.

J Cell Mol Med ; 26(21): 5403-5413, 2022 11.

Article em En | MEDLINE | ID: mdl-36226571

Assuntos

Doença de von Willebrand Tipo 2; Doenças de von Willebrand; Masculino; Humanos; Fator de von Willebrand/genética; Linhagem; Sêmen/metabolismo; Doenças de von Willebrand/genética

Palavras-chave

de novo variant; type 2 von Willebrand disease; von Willebrand disease

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças de von Willebrand / Doença de von Willebrand Tipo 2 Tipo de estudo: Prognostic_studies Limite: Humans / Male Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google