Publications by authors named "R Mahima"

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SLC18A2 associated infantile-onset- parkinsonism-dystonia 2: A novel genotype.
Akshaya Janardhanan, Rohan Mahale, R Mahima, Shilpi Goyal, Bhavana Chanda

Parkinsonism Relat Disord· August 2025

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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.
Subasree Ramakrishnan, Faheem Arshad, B S Keerthana, Susan Bosco, Arun Gokul Pon, R Mahima

BMC Neurol· August 2025

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