New Assay of Detecting Common Mutation Causing Sanjad-Sakati Syndrome Using Real-Time Fluorescence PCR and Melting Curve Analysis
Mohamed H. Al-Hamed, Haya Al-Jurayb & Faiqa Imtiaz · Journal of Applied Life Sciences International · 2014
Sanjad-Sakati Syndrome (SSS) is an autosomal recessive disorder reported mainly in Middle Eastern populations. The mutation c.155_166del in exon 3 of the TBCE gene is the most common cause of SSS in the population. Each double stranded DNA product has a specific melting temperatu...
Open access
Research Article
10.9734/JALSI/2015/13103