Imaging in cutis laxa syndrome caused by a dominant negative ALDH18A1 mutation, with hypotheses for intracranial vascular tortuosity and wide perivascular spaces

P. F. Sinnige, C. M. A. van Rauenswaaij-Arts, P. Caruso, A. E. Lin, M. Boon, E. Rahikkala, B. Callewaert, L. C. Meiners*

*Corresponding author for this work

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Medicine and Dentistry

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