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A novel mutation in the sulfate transporter gene SLC26A2 (DTDST) specific to the Finnish population causes de la Chapelle dysplasia
  1. 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
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Citation

Bonafé L, Hästbacka J, de la Chapelle A, et al
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

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