How to Cite this Article: Zampatti S, Castori M, Fischer B, Ferrari P, Garavelli L, Dionisi-Vici C, Agolini E, Wischmeijer A, Morava E, Novelli G, Häberle J, Kornak U, Brancati F. 2012. De Barsy Syndrome: a genetically heterogeneous autosomal recessive cutis laxa syndrome related to P5CS and PYCR1 dysfunction. Am J Med Genet Part A 158A:927–931.
De Barsy Syndrome: A genetically heterogeneous autosomal recessive cutis laxa syndrome related to P5CS and PYCR1 dysfunction†
Article first published online: 12 MAR 2012
Copyright © 2012 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Volume 158A, Issue 4, pages 927–931, April 2012
How to Cite
Zampatti, S., Castori, M., Fischer, B., Ferrari, P., Garavelli, L., Dionisi-Vici, C., Agolini, E., Wischmeijer, A., Morava, E., Novelli, G., Häberle, J., Kornak, U. and Brancati, F. (2012), De Barsy Syndrome: A genetically heterogeneous autosomal recessive cutis laxa syndrome related to P5CS and PYCR1 dysfunction. Am. J. Med. Genet., 158A: 927–931. doi: 10.1002/ajmg.a.35231
- Issue published online: 23 MAR 2012
- Article first published online: 12 MAR 2012
- Manuscript Accepted: 14 DEC 2011
- Manuscript Received: 31 AUG 2011
- Italian Ministry of Health (Ricerca Corrente 2011)
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