Twenty patients including 7 probands with autosomal dominant cutis laxi confirm clinical and molecular homogeneity

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Publication year
2013
Author(s)
Hadj-Rabia, S.
Callewaert, B.L.
Bourrat, E.
Kempers, M.J.E.
Plomp, A.S.
Layet, V.
Bartholdi, D.
Renard, M.
Backer, J.D.
Malfait, F.
Vanakker, O.M.
Couke, P.J.
Paepe, A.M. De
Bodemer, C.
Source
Orphanet Journal of Rare Diseases, 8, 1, (2013), pp. 36
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DOI
Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/117902   https://hdl.handle.net/2066/117902
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