APA

Sinnige P. F., van Ravenswaaij-Arts C. M. A., Caruso P., Lin A. E., Boon M., Rahikkala E., Callewaert B. & Meiners L. C. (20180509). Imaging in cutis laxa syndrome caused by a dominant negative ALDH18A1 mutation, with hypotheses for intracranial vascular tortuosity and wide perivascular spaces. : European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Chicago

Sinnige P F, van Ravenswaaij-Arts C M A, Caruso P, Lin A E, Boon M, Rahikkala E, Callewaert B and Meiners L C. 20180509. Imaging in cutis laxa syndrome caused by a dominant negative ALDH18A1 mutation, with hypotheses for intracranial vascular tortuosity and wide perivascular spaces. : European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Harvard

Sinnige P. F., van Ravenswaaij-Arts C. M. A., Caruso P., Lin A. E., Boon M., Rahikkala E., Callewaert B. and Meiners L. C. (20180509). Imaging in cutis laxa syndrome caused by a dominant negative ALDH18A1 mutation, with hypotheses for intracranial vascular tortuosity and wide perivascular spaces. : European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

MLA

Sinnige P F, van Ravenswaaij-Arts C M A, Caruso P, Lin A E, Boon M, Rahikkala E, Callewaert B and Meiners L C. Imaging in cutis laxa syndrome caused by a dominant negative ALDH18A1 mutation, with hypotheses for intracranial vascular tortuosity and wide perivascular spaces. : European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society. 20180509.