Twenty patients including 7 probands with autosomal dominant cutis laxa confirm clinical and molecular homogeneity.
Data and Resources
Additional Info
| Field | Value |
|---|---|
| Source | ISSN: 1750-1172 |
| Author | Hadj-Rabia, Smail, Callewaert, Bert, Bourrat, Emmanuelle, Kempers, Marlies, Plomp, Astrid, Layet, Valerie, Bartholdi, Deborah, Renard, Marjolijn, Backer, Julie De, Malfait, Fransiska, Vanakker, Olivier, Coucke, Paul, de Paepe, Anne, Bodemer, Christine |
| Maintainer | CCSD |
| Last Updated | May 13, 2026, 06:57 (UTC) |
| Created | May 13, 2026, 06:57 (UTC) |
| Identifier | inserm-00798332 |
| Language | en |
| Rights | https://about.hal.science/hal-authorisation-v1/ |
| contributor | Génétique et épigénétique des maladies métaboliques, neurosensorielles et du développement (Inserm U781) ; Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM) |
| creator | Hadj-Rabia, Smail |
| date | 2013-02-25T00:00:00 |
| harvest_object_id | f6630d9f-1a47-4f52-94d7-47b2f6f798ed |
| harvest_source_id | 3374d638-d20b-4672-ba96-a23232d55657 |
| harvest_source_title | test moissonnage SELUNE |
| metadata_modified | 2025-07-10T00:00:00 |
| relation | info:eu-repo/semantics/altIdentifier/doi/10.1186/1750-1172-8-36 |
| set_spec | type:ART |