Whole Genome Sequencing identifies novel structural variant in a large Indian family affected with X - linked agammaglobulinemia
Abhinav K. Jain, Geeta Madathil Govindaraj, Athulya Edavazhippurath, Nabeel Valappil Faisal, Rahul C. Bhoyar, Vishu Gupta, Ramya Uppuluri, Shiny Padinjarayil Manakkad, Atul Kashyap, Anoop Kumar, Mohit Kumar Divakar, Mohamed Imran, Sneha Sawant, Aparna Dhondi Dalvi, Krishnan Chakkiyar, , Vinod Scaria
The paper identifies a novel 5,296 bp deletion in the BTK gene in an Indian family with X-linked agammaglobulinemia through whole genome sequencing and carrier screening.
PLoS ONE · Jul 12, 2021Peer-reviewedGenetic & Genomic Medicine