Fanconi Anaemia is a rare, genetic heterogeneous multisystem disease that is the most
common congenital syndrome of marrow failure. Twenty genes have been reported to cause …

La anemia de Fanconi es una enfermedad hereditaria con patrón de transmisión
autosómico recesivo, asociada con múltiples mutaciones en al menos 20 genes cuyos …

Fanconi anemia is a hereditary disease with an autosomal recessive transmission pattern,
associated with multiple mutations on at least 20 genes whose products are part of the cell's …

Además de ser indispensable para la vida, el agua es un elemento notable dotado de
sorprendentes propiedades; es el mayor componente del cuerpo humano (entre 65 y 70 …

Abstract Background and Objective: Fanconi anemia (FA) patients have a reduced ability to
form blood cells, accompanied by multiple congenital malformations, mental retardation …

Background Gene therapy approaches for the treatment of Fanconi anemia (FA) hold
promise for patients without a suitably matched donor for an allogeneic bone marrow …

Hematopoietic stem cells (HSCs) are rare cells that reside in bone marrow. HSCs function to
give rise to all blood cells through proliferation and differentiation, but also to HSCs in a …