Truncation of the E3 ubiquitin ligase component FBXO31 causes non-syndromic autosomal recessive intellectual disability in a Pakistani family
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, SVolume:
133
Language:
english
Journal:
Human Genetics
DOI:
10.1007/s00439-014-1438-0
Date:
August, 2014
File:
PDF, 591 KB
english, 2014