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 |