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Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia

✍ Scribed by Nürnberg, Peter; Thiele, Holger; Chandler, David; Höhne, Wolfgang; Cunningham, Michael L.; Ritter, Heide; Leschik, Gundula; Uhlmann, Karen; Mischung, Claudia; Harrop, Karen

Book ID: 109915798
Publisher: Nature Publishing Group
Year: 2001
Tongue: English
Weight: 758 KB
Volume: 28
Category: Article
ISSN: 1061-4036
DOI: 10.1038/ng0501-37

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