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    SOX10 mutations in patients with Waardenburg-Hirschsprung disease

    Waardenburg syndrome (WS; deafness with pigmentary abnormalities) and Hirschsprung's disease (HSCR; aganglionic megacolon) are congenital disorders caused by defective function of the embryonic neural crest1,2. W...

    Véronique **ault, Nadège Bondurand, Kirsten Kuhlbrodt, Derk E. Goerich… in Nature Genetics (1998)