How to cite this article: Kornak U, Brancati F, Le Merrer M, Lichtenbelt K, Höhne W, Tinschert S, Garaci FG, Dallapiccola B, Nürnberg P. 2010. Three novel mutations in the ANK membrane protein cause craniometaphyseal dysplasia with variable conductive hearing loss. Am J Med Genet Part A 152A:870–874.
Three novel mutations in the ANK membrane protein cause craniometaphyseal dysplasia with variable conductive hearing loss†
Article first published online: 26 MAR 2010
Copyright © 2010 Wiley-Liss, Inc.
American Journal of Medical Genetics Part A
Volume 152A, Issue 4, pages 870–874, April 2010
How to Cite
Kornak, U., Brancati, F., Le Merrer, M., Lichtenbelt, K., Höhne, W., Tinschert, S., Garaci, F. G., Dallapiccola, B. and Nürnberg, P. (2010), Three novel mutations in the ANK membrane protein cause craniometaphyseal dysplasia with variable conductive hearing loss. Am. J. Med. Genet., 152A: 870–874. doi: 10.1002/ajmg.a.33301
- Issue published online: 26 MAR 2010
- Article first published online: 26 MAR 2010
- Manuscript Accepted: 12 DEC 2009
- Manuscript Received: 16 DEC 2008
- Deutsche Forschungsgemeinschaft (Collaborative Research Centre 577)
- Italian Ministry of Health (Ricerca Corrente 2009)
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