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APA Citation
Sinnige, P., van Ravenswaaij-Arts, C., Caruso, P., Lin, A., Boon, M., Rahikkala, E., Callewaert, B., & Meiners, L. (n.d.). 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, 21, 912–920. http://access.bl.uk/ark:/81055/vdc_100050156653.0x000027