How to Cite this Article: Verhagen JMA, Huijmans JG, Williams M, van Ruyven RLJ, Bergen AAB, Wouters CH, Brooks AS. 2012. Incidental finding of alpha-methylacyl-CoA racemase deficiency in a patient with oculocutaneous albinism type 4. Am J Med Genet Part A 158A: 2931–2934.
Article first published online: 17 SEP 2012
Copyright © 2012 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Special Issue: SPECIAL ISSUE: GROWTH CHARTS IN GENETIC SYNDROMES
Volume 158A, Issue 11, pages 2931–2934, November 2012
How to Cite
Verhagen, J. M.A., Huijmans, J. G., Williams, M., van Ruyven, R. L.J., Bergen, A. A.B., Wouters, C. H. and Brooks, A. S. (2012), Incidental finding of alpha-methylacyl-CoA racemase deficiency in a patient with oculocutaneous albinism type 4. Am. J. Med. Genet., 158A: 2931–2934. doi: 10.1002/ajmg.a.35611
Conflict of interest: Nothing to declare.
- Issue published online: 17 OCT 2012
- Article first published online: 17 SEP 2012
- Manuscript Accepted: 17 JUL 2012
- Manuscript Received: 26 APR 2012
Additional Supporting Information may be found in the online version of this article.
Please note: Wiley Blackwell is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.