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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
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2002 (English)In: Br J Haematol, Vol. 119, no 1, p. 261-4Article in journal (Refereed) Published
Abstract [en]

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, we investigated the segregation of markers spanning the RPS19 gene region on chromosome 19q13.2 and performed sequence analysis of all exons in the RPS19 gene in seven TEC sibling pairs. Linkage analysis supported allelism for TEC and DBA at the RPS19 gene locus and implies molecular mechanisms other than structural mutations in the RPS19 gene.

Place, publisher, year, edition, pages
2002. Vol. 119, no 1, p. 261-4
Keywords [en]
Adult, Child, Chromosomes; Human; Pair 19/*genetics, Erythroblasts, Genotype, Hematologic Diseases/*genetics, Humans, Linkage (Genetics)/genetics, Mutation/genetics, Pedigree, Research Support; Non-U.S. Gov't, Ribosomal Proteins/*genetics, Sequence Analysis
National Category
Medical Genetics
Research subject
Molecular Genetics
Identifiers
URN: urn:nbn:se:uu:diva-373435OAI: oai:DiVA.org:uu-373435DiVA, id: diva2:1301238
Conference
2005-09-20T18:44:00.000+02:00
Note

article; 2016-02-29T12:57:49.774+01:00

Available from: 2019-04-01 Created: 2019-04-01 Last updated: 2019-04-01

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