Journal article
Twenty patients including 7 probands with autosomal dominant cutis laxa confirm clinical and molecular homogeneity
- Hadj-Rabia, Smail
- Callewaert, Bert L
- Bourrat, Emmanuelle
- Kempers, Marlies
- Plomp, Astrid S
- Layet, Valerie
- Bartholdi, Deborah
- Renard, Marjolijn
- Backer, Julie De
- Malfait, Fransiska
- Vanakker, Olivier M
- Coucke, Paul J
- De Paepe, Anne M
- Bodemer, Christine
Published in:
- Orphanet Journal of Rare Diseases. - Springer Science and Business Media LLC. - 2013, vol. 8, no. 1, p. 36
- Language
-
- English
- Open access status
- gold
- Identifiers
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- DOI 10.1186/1750-1172-8-36
- ISSN 1750-1172
- Persistent URL
- https://sonar.ch/global/documents/216797
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