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

Judith Verhagen, Jan Huijmans, Monique Williams, RLJ van Ruyven, Arthur Bergen, Cokkie Wouters, Alice Brooks

Research output: Contribution to journalArticleAcademicpeer-review

6 Citations (Scopus)
Original languageUndefined/Unknown
Pages (from-to)2931-2934
Number of pages4
JournalAmerican Journal of Medical Genetics
Volume158A
DOIs
Publication statusPublished - 2012

Research programs

  • EMC MGC-02-96-01
  • EMC MM-01-54-01

Cite this