A carregar...
MxA overexpression reveals a common genetic link in four Fanconi anemia complementation groups.
Fanconi anemia (FA) consists of a group of at least five autosomal recessive disorders that share both clinical (e.g., birth defects and hematopoietic failure) and cellular (e.g., sensitivity to cross-linking agents and predisposition to apoptosis) features with each other. However, a common pathoge...
Na minha lista:
| Publicado no: | J Clin Invest |
|---|---|
| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Clinical Investigation
1997
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC508494/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9389754/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI119836 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|