Incidental finding of alpha-methylacyl-CoA racemase deficiency in a patient with oculocutaneous albinism type 4.

J.M. Verhagen, J.G. Huijmans, M. Williams, R.L. Van Ruijven, A.A.B. Bergen, C.H. Wouters, A.S. Brooks

Research output: Contribution to journal/periodicalArticleScientificpeer-review

12 Citations (Scopus)
Original languageEnglish
Pages (from-to)2931-2934
JournalAmerican Journal of Medical Genetics A
Volume158A
DOIs
Publication statusPublished - 2012

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