Clinical profile, atrophy and inheritance patterns of pathogenic MAPT gene mutations in Frontotemporal dementia detected using whole exome sequencing: a single-center first report from India - Ramakrishnan, Subasree; Arshad, Faheem; Keerthana, B. S.; Bosco, Susan; Gokul Pon, Arun; Ganaraja, V. H.; Madhusudhan, Deekshitha; Mahima, R.; Arunachal, Gautham; Kulanthaivelu, Karthick; Alladi, Suvarna (BMC neurology, 2025)
Keywords: Development and progression; Gene mutations; Genes; Genetic aspects; Nervous system diseases; India