Miller (GeneWiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODH

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Miller (GeneWiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODH

Author: Rainger, Joe; Bengani, Hemant; Campbell, Leigh; Anderson, Eve; Sokhi, Kishan; Lam, Wayne; Riess, Angelika; Ansari, Morad; Smithson, Sarah; Lees, Melissa; Mercer, Catherine; McKenzie, Kathryn; Lengfeld, Tobias; Gener Querol, Blanca; Branney, Peter; McKay, Stewart; Morrison, Harris; Medina, Bethan; Robertson, Morag; Kohlhase, Juergen; Gordon, Colin; Kirk, Jean; Wieczorek, Dagmar; FitzPatrick, David R.
Tübinger Autor(en):
Rieß, Angelika
Published in: Human Molecular Genetics (2012), Bd. 21, H. 18, S. 3969-3983
Verlagsangabe: Oxford Univ Press
Language: English
Full text: http://dx.doi.org/10.1093/hmg/dds218
ISSN: 0964-6906
DDC Classifikation: 570 - Life sciences; biology
610 - Medicine and health
Dokumentart: Artikel
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