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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.

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Title: 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.
Authors: Ramakrishnan, Subasree1 (AUTHOR) subasree.ramakrishnan@gmail.com, Arshad, Faheem1 (AUTHOR) faheem2285@gmail.com, Keerthana, B. S.1 (AUTHOR) keerthanabs095@gmail.com, Bosco, Susan1 (AUTHOR) susanbosco273@gmail.com, Gokul Pon, Arun1 (AUTHOR) arungokulpon@gmail.com, Ganaraja, V. H.1 (AUTHOR) ganaraj.v.h.91@gmail.com, Madhusudhan, Deekshitha2 (AUTHOR) deekshitha82@gmail.com, Mahima, R.2 (AUTHOR) mahima.rp99@gmail.com, Arunachal, Gautham2 (AUTHOR) gautam.arunachal@gmail.com, Kulanthaivelu, Karthick3 (AUTHOR) pammalkk@gmail.com, Alladi, Suvarna1 (AUTHOR) alladisuvarna@hotmail.com
Source: BMC Neurology. 8/27/2025, Vol. 25 Issue 1, p1-13. 13p.
Database: Academic Search Ultimate
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  Data: 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.
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  Data: <searchLink fieldCode="JN" term="%22BMC+Neurology%22">BMC Neurology</searchLink>. 8/27/2025, Vol. 25 Issue 1, p1-13. 13p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=187619635
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