A carregar...

Targeted mutation of zebrafish fga models human congenital afibrinogenemia

Mutations in the human fibrinogen genes can lead to the absence of circulating fibrinogen and cause congenital afibrinogenemia. This rare bleeding disorder is associated with a variable phenotype, which may be influenced by environment and genotype. Here, we present a zebrafish model of afibrinogene...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Fish, Richard J., Di Sanza, Corinne, Neerman-Arbez, Marguerite
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Hematology 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3975262/
https://ncbi.nlm.nih.gov/pubmed/24553182
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2013-12-547182
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!