Article
Familial transient erythroblastopenia of childhood is associated with the chromosome 19q13.2 region but not caused by mutations in coding sequences of the ribosomal protein S19 (RPS19) gene.
British journal of haematology - 1 Oct 2002
Gustavsson Peter, Klar Joakim, Matsson Hans, Forestier Erik, Henter Jan-Inge, Rao Sreedhar, Seip Martin, Skeppner Gunnar, Dahl Niklas
Abstract excerpt
Transient erythroblastopenia of childhood (TEC) is a rare condition, which at onset may be difficult to distinguish from Diamond-Blackfan anaemia (DBA). We have previously shown that mutations in the ribosomal protein S19 gene (RPS19) cause DBA. In order to clarify whether TEC and DBA are allelic...
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