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 journal › Article › Academic › peer-review

12 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	2931-2934
Number of pages	4
Journal	American Journal of Medical Genetics
Volume	158A
DOIs	https://doi.org/10.1002/ajmg.a.35611
Publication status	Published - 2012

Research programs

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

author = "Judith Verhagen and Jan Huijmans and Monique Williams and {van Ruyven}, RLJ and Arthur Bergen and Cokkie Wouters and Alice Brooks",

year = "2012",

doi = "10.1002/ajmg.a.35611",

language = "Undefined/Unknown",

volume = "158A",

pages = "2931--2934",

journal = "American Journal of Medical Genetics",

issn = "0148-7299",

publisher = "Wiley-Liss Inc.",

}

TY - JOUR

T1 - Incidental finding of alpha-methylacyl-CoA racemase deficiency in a patient with oculocutaneous albinism type 4

AU - Verhagen, Judith

AU - Huijmans, Jan

AU - Williams, Monique

AU - van Ruyven, RLJ

AU - Bergen, Arthur

AU - Wouters, Cokkie

AU - Brooks, Alice

PY - 2012

Y1 - 2012

U2 - 10.1002/ajmg.a.35611

DO - 10.1002/ajmg.a.35611

M3 - Article

C2 - 22987308

SN - 0148-7299

VL - 158A

SP - 2931

EP - 2934

JO - American Journal of Medical Genetics

JF - American Journal of Medical Genetics

ER -