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Date 2017 Author/Creator Lin, A.E.

1. Imaging in cutis laxa syndrome caused by a dominant negative ALDH18A1 mutation, with hypotheses for intracranial vascular tortuosity and wide perivascular spaces. (November 2017)

Authors:
Sinnige, P.F.; van Ravenswaaij-Arts, C.M.A.; Caruso, P.; Lin, A.E.; Boon, M.; Rahikkala, E.; Callewaert, B.; Meiners, L.C.
Journal:
European journal of paediatric neurology
Issue:
Volume 21:Number 6(2017:Nov.)
Page Start:
912
Record Type:
Journal Article
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