SOX10 mutations in patients with Waardenburg-Hirschsprung disease

Nature Genetics

Volumn 18, Issue 2, 1998, Pages 171-173

  Pingault, Véronique ^a   Bondurand, Nadège ^a   Kuhlbrodt, Kirsten ^b   Goerich, Derk E ^b   Préhu, Marie Odette ^a   Puliti, Aldamaria ^a,e   Herbarth, Beate ^b   Hermans Borgmeyer, Irm ^b   Legius, Eric ^c   Matthijs, Gert ^c   Amiel, Jeanne ^d   Lyonnet, Stanislas ^d   Ceccherini, Isabella ^e   Romeo, Giovanni ^e   Smith, Jill Clayton ^f   Read, Andrew P ^f   Wegner, Michael ^b   Goossens, Michel ^a  

^a HENRI MONDOR HOSPITAL   (France)

^b UNIVERSITY OF HAMBURG   (Germany)

^c UNIVERSITY OF LEUVEN   (Belgium)

^d HÔPITAL NECKER ENFANTS MALADES   (France)

^e G GASLINI INSTITUTE   (Italy)

^f ST MARY S HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; DNA SEQUENCE; GENE MUTATION; GENE SEQUENCE; HIRSCHSPRUNG DISEASE; MICROPHTHALMIA; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SEQUENCE HOMOLOGY; WAARDENBURG SYNDROME;

EID: 17344366171     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng0298-171     Document Type: Article

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