Inherited thrombocytopenias are heterogeneous diseases caused by at least 20 genes playing different role in the processes of megakaryopoiesis and platelet production. Some forms, such as thrombocytopenia 4 (THC4), are very rare and not well characterized. THC4 is an autosomal dominant mild thrombocytopenia described in only one large family fromNewZealand and due to amutation (G41S) of the somatic isoform of the cytochrome c (CYCS) gene. We report a novel CYCS mutation (Y48H) in patients from an Italian family. Similar to individuals carrying G41S, they have platelets of normal size and morphology, which are only partially reduced in number, but no prolonged bleeding episodes. In order to determine the pathogenetic consequences of Y48H, we...
<div><p>The naturally occurring human cytochrome <i>c</i> variant (G41S) is associated with a mild a...
The naturally occurring human cytochrome c variant (G41S) is associated with a mild autoso-mal domin...
Mutation of cytochrome c in humans causes mild autosomal dominant thrombocytopenia. The role of cyto...
Inherited thrombocytopenias are heterogeneous diseases caused by at least 20 genes playing different...
Inherited thrombocytopenias are heterogeneous diseases caused by at least 20 genes playing different...
Inherited thrombocytopenias are heterogeneous diseases caused by at least 20genes playing different ...
Inherited thrombocytopenias are heterogeneous diseases caused by at least 20 genes playing different...
AbstractInherited thrombocytopenias are heterogeneous diseases caused by at least 20 genes playing d...
Inherited thrombocytopenias are heterogeneous diseases caused by at least 20 genes playing different...
Inherited thrombocytopenias are heterogeneous diseases caused by at least 20 genes playing different...
The first naturally occurring mutation identified in the highly conserved cytochrome c protein was d...
Thrombocytopenia Cargeeg is a rare autosomal dominant disorder identified in a New Zealand family wi...
The naturally occurring human cytochrome c variant (G41S) is associated with a mild autosomal domina...
The naturally occurring human cytochrome c variant (G41S) is associated with a mild autosomal domina...
The only known naturally occurring mutation in cytochrome c, identified in a New Zealand family, is ...
<div><p>The naturally occurring human cytochrome <i>c</i> variant (G41S) is associated with a mild a...
The naturally occurring human cytochrome c variant (G41S) is associated with a mild autoso-mal domin...
Mutation of cytochrome c in humans causes mild autosomal dominant thrombocytopenia. The role of cyto...
Inherited thrombocytopenias are heterogeneous diseases caused by at least 20 genes playing different...
Inherited thrombocytopenias are heterogeneous diseases caused by at least 20 genes playing different...
Inherited thrombocytopenias are heterogeneous diseases caused by at least 20genes playing different ...
Inherited thrombocytopenias are heterogeneous diseases caused by at least 20 genes playing different...
AbstractInherited thrombocytopenias are heterogeneous diseases caused by at least 20 genes playing d...
Inherited thrombocytopenias are heterogeneous diseases caused by at least 20 genes playing different...
Inherited thrombocytopenias are heterogeneous diseases caused by at least 20 genes playing different...
The first naturally occurring mutation identified in the highly conserved cytochrome c protein was d...
Thrombocytopenia Cargeeg is a rare autosomal dominant disorder identified in a New Zealand family wi...
The naturally occurring human cytochrome c variant (G41S) is associated with a mild autosomal domina...
The naturally occurring human cytochrome c variant (G41S) is associated with a mild autosomal domina...
The only known naturally occurring mutation in cytochrome c, identified in a New Zealand family, is ...
<div><p>The naturally occurring human cytochrome <i>c</i> variant (G41S) is associated with a mild a...
The naturally occurring human cytochrome c variant (G41S) is associated with a mild autoso-mal domin...
Mutation of cytochrome c in humans causes mild autosomal dominant thrombocytopenia. The role of cyto...