Cutis laxa and excessive bone growth due to de novo mutations in PTDSS1

The cutis laxa syndromes are multisystem disorders that share loose redundant inelastic and wrinkled skin as a common hallmark clinical feature. The underlying molecular defects are heterogeneous and 13 different genes have been involved until now, all of them being implicated in elastic fiber assem...

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Detalles Bibliográficos
Autores principales: Piard, Juliette, Lespinasse, James, Vlckova, Marketa, Mensah, Martin A., Iurian, Sorin, Simandlova, Martina, Malikova, Marcela, Bartsch, Oliver, Rossi, Massimiliano, Lenoir, Marion, Nugues, Frédérique, Mundlos, Stefan, Kornak, Uwe, Stanier, Philip, Sousa, Sérgio B., Van Maldergem, Lionel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Clinical Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5838527/
https://www.ncbi.nlm.nih.gov/pubmed/29341480
http://dx.doi.org/10.1002/ajmg.a.38604

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5838527/
https://www.ncbi.nlm.nih.gov/pubmed/29341480
http://dx.doi.org/10.1002/ajmg.a.38604

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