Article info
Letters to JMG
A novel mutation in the sulfate transporter gene SLC26A2 (DTDST) specific to the Finnish population causes de la Chapelle dysplasia
- Dr Luisa Bonafé, Division of Molecular Pediatrics, Centre Hospitalier Universitaire Vaudois, Clinique Infantile 02-35, Av. P. Decker 2, 1011 – Lausanne, Switzerland; Luisa.Bonafe{at}chuv.ch
Citation
A novel mutation in the sulfate transporter gene SLC26A2 (DTDST) specific to the Finnish population causes de la Chapelle dysplasia
Publication history
- Received January 12, 2008
- Revised June 25, 2008
- Accepted July 21, 2008
- First published August 15, 2008.
Online issue publication
December 01, 2008
Article Versions
- Previous version (15 August 2008).
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2008 BMJ Publishing Group