Twenty patients including 7 probands with autosomal dominant cutis laxa confirm clinical and molecular homogeneity.
| Autor: | Hadj-Rabia, Smail1 smail.hadj@inserm.fr, Callewaert, Bert L.2 Bert.Callewaert@Ugent.be, Bourrat, Emmanuelle3, Kempers, Marlies4, Plomp, Astrid S.5, Layet, Valerie6, Bartholdi, Deborah7, Renard, Marjolijn2, Backer, Julie De2, Malfait, Fransiska2, Vanakker, Olivier M.2, Coucke, Paul J.2, De Paepe, Anne M.2, Bodemer, Christine1 |
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| Zdroj: | Orphanet Journal of Rare Diseases. 2013, Vol. 8 Issue 1, p1-8. 8p. 1 Color Photograph, 1 Diagram, 4 Charts. |
| Databáze: | Academic Search Ultimate |
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