12881_2020_998_MOESM1_ESM.docx (19.23 kB)
Additional file 1 of Novel variants underlying autosomal recessive intellectual disability in Pakistani consanguineous families
journal contribution
posted on 2020-03-25, 04:32 authored by Muhammad Ilyas, Stephanie Efthymiou, Vincenzo Salpietro, Nuzhat Noureen, Faisal Zafar, Sobiah Rauf, Asif Mir, Henry HouldenAdditional file 1: Supplementary Table 1. List of Primers used for Segregation analysis. Supplementary Table 2. Exome sequencing Family MR-4 two Patients revealed VPS53 Mutation. Supplementary Table 3. Exome sequencing Family MR-7 two Patients revealed GLB1 Mutation. Supplementary Table 4. Exome sequencing Family MR-8 one Patients revealed MLC1 gene Mutation.