دورية أكاديمية

Dominant ?-catenin mutations cause intellectual disability with recognizable syndromic features

التفاصيل البيبلوغرافية
العنوان: Dominant ?-catenin mutations cause intellectual disability with recognizable syndromic features
المؤلفون: Tucci, Valter, Kleefstra, Tjitske, Hardy, Andrea, Heise, Ines, Maggi, Silvia, Willemsen, Marjolein H., Hilton, Helen, Esapa, Chris, Simon, Michelle, Buenavista, Maria-Teresa, McGuffin, Liam J., Vizor, Lucie, Dodero, Luca, Tsaftaris, Sotirios, Romero, Rosario, Nillesen, Willy N., Vissers, Lisenka E.L.M., Kempers, Marlies J., Vulto-van Silfhout, Anneke T., Iqbal, Zafar, Orlando, Marta, Maccione, Alessandro, Lassi, Glenda, Farisello, Pasqualina, Contestabile, Andrea, Tinarelli, Federico, Nieus, Thierry, Raimondi, Andrea, Greco, Barbara, Cantatore, Daniela, Gasparini, Laura, Berdondini, Luca, Bifone, Angelo, Gozzi, Alessandro, Wells, Sara, Nolan, Patrick M.
بيانات النشر: American Society for Clinical Investigation
سنة النشر: 2014
المجموعة: University of Nottingham: Repository@Nottingham
نوع الوثيقة: article in journal/newspaper
اللغة: unknown
تدمد: 0021-9738
العلاقة: https://nottingham-repository.worktribe.com/output/3056696Test; Journal of Clinical Investigation; Volume 124; Issue 4; Pagination 1468-1482; https://nottingham-repository.worktribe.com/file/3056696/1/Tucci2014_JCITest
DOI: 10.1172/jci70372
الإتاحة: https://doi.org/10.1172/jci70372Test
https://nottingham-repository.worktribe.com/file/3056696/1/Tucci2014_JCITest
https://nottingham-repository.worktribe.com/output/3056696Test
حقوق: openAccess
رقم الانضمام: edsbas.439388ED
قاعدة البيانات: BASE