WFS1 Gene–associated Diabetes Phenotypes and Identification of a Founder Mutation in Southern India - Chapla, Aaron; Johnson, Jabasteen; Korula, Sophy; Mohan, Nisha; Ahmed, Anish; Varghese, Deny; Rangasamy, Parthiban; Ravichandran, Lavanya; Jebasingh, Felix; Kumar Agrawal, Krishna; Somasundaram, Noel; Hesarghatta Shyamasunder, Asha; et al. (The journal of clinical endocrinology and metabolism, 2022)
Keywords: Analysis; Atrophy; Deafness; Diabetes; Diabetes insipidus; Diagnosis; DNA sequencing; Female; Founder effect; Genes; Genetic aspects; Genetic screening; Haplotypes; Hereditary diseases; Humans; India - epidemiology; Male; Medical screening; Membrane Proteins - genetics; Mutation; Neurodegeneration; Next-generation sequencing; Nucleotide sequencing; Optic atrophy; Phenotype; Phenotypes; Type 2 diabetes; Wolfram Syndrome - diagnosis; Wolfram Syndrome - genetics; Wolfram Syndrome - pathology; India; Wolfram syndrome; next-generation sequencing; founder mutation; DIDMOAD; WFS1