دورية أكاديمية
Truncation of the E3 ubiquitin ligase component FBXO31 causes non-syndromic autosomal recessive intellectual disability in a Pakistani family
| العنوان: | Truncation of the E3 ubiquitin ligase component FBXO31 causes non-syndromic autosomal recessive intellectual disability in a Pakistani family |
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| المؤلفون: | Mir, Asif, Sritharan, Kumudesh, Mittal, Kirti, Vasli, Nasim, Araujo, Carolina, Jamil, Talal, Rafiq, Muhammad Arshad, Anwar, Zubair, Mikhailov, Anna, Rauf, Sobiah, Mahmood, Huda, Shakoor, Abdul, Ali, Sabir, So, Joyce, Naeem, Farooq, Ayub, Muhammad, Vincent, John B. |
| المصدر: | Human Genetics. August 2014 133(8):975-984 |
| قاعدة البيانات: | Springer Nature Journals |
Find this article in full text from Springer Verlag. 
Full Text Finder | تدمد: | 03406717 14321203 |
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| DOI: | 10.1007/s00439-014-1438-0 |