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
利用全外显子组测序检测额颞叶痴呆中致病性MAPT基因突变的临床特征、萎缩和遗传模式：来自印度的单中心首例报告
期刊:BMC Neurology
影响因子:2.2
doi:10.1186/s12883-025-04336-9
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
