A novel deletion mutation in the <it>TUSC3 </it>gene in a consanguineous Pakistani family with autosomal recessive nonsyndromic intellectual disability

• Glavni autori: Ali Nadir (Autor), Noor Abdul (Autor), Rafiq Muhammad (Autor), Khan Muzammil (Autor), Ali Ghazanfar (Autor), Vincent John B (Autor), Ansar Muhammad (Autor)
• Format: Knjiga
• Izdano: BMC, 2011-04-01T00:00:00Z.
• Teme: article
• Online pristup: Connect to this object online.

<p>Abstract</p> <p>Background</p> <p>Intellectual disability (ID) is a serious disorder of the central nervous system with a prevalence of 1-3% in a general population. In the past decades, the research focus has been predominantly on X-linked ID (68 loci and 19 genes f...