A carregar...

JAK2 mutations to the fore in hereditary thrombocythemia

Acquired mutations of the gene that encodes the intracellular signalling molecule JAK2 are the most frequently observed disease-driving events of the common myeloproliferative neoplasms. A number of germline JAK2 mutations have recently been described in several kindred with the rare disease of here...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:JAKSTAT
Autor principal: Langabeer, Stephen E
Formato: Artigo
Idioma:Inglês
Publicado em: Taylor & Francis 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4580080/
https://ncbi.nlm.nih.gov/pubmed/26413420
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/21623988.2014.957618
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!