APA (7th ed.) Citation

Ramakrishnan, S., Arshad, F., Keerthana, B. S., Bosco, S., Gokul Pon, A., Ganaraja, V. H., . . . Alladi, S. (2025). 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. BMC neurology, 25(1), . https://doi.org/10.1186/s12883-025-04336-9

Chicago Style (17th ed.) Citation

Ramakrishnan, Subasree, et al. "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." BMC Neurology 25, no. 1 (2025). https://doi.org/10.1186/s12883-025-04336-9.

MLA (9th ed.) Citation

Ramakrishnan, Subasree, et al. "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." BMC Neurology, vol. 25, no. 1, 2025, https://doi.org/10.1186/s12883-025-04336-9.