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HARVARD Citation
Bonafé, L. et al. (2008). A novel mutation in the sulfate transporter gene SLC26A2 (DTDST) specific to the Finnish population causes de la Chapelle dysplasia. Journal of medical genetics. 45 (12), pp. 827-831. [Online].
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Bonafé, L. et al. (2008). A novel mutation in the sulfate transporter gene SLC26A2 (DTDST) specific to the Finnish population causes de la Chapelle dysplasia. Journal of medical genetics. 45 (12), pp. 827-831. [Online].