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A Novel Rare Homozygous R47C Variant in TREM2 with Frontal Variant Alzheimer's Disease.

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Bibliographic Details
Title:	A Novel Rare Homozygous R47C Variant in TREM2 with Frontal Variant Alzheimer's Disease.
Authors:	Mallika AP; Human Molecular Genetics, Rajiv Gandhi Centre for Biotechnology, Trivandrum, Kerala, India.; Cognition and Behavioral Neurology Section, Department of Neurology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, Kerala, India.; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA., Mathuranath PS; Cognition and Behavioral Neurology Section, Department of Neurology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, Kerala, India.; Department of Neurology, National Institute of Mental Health and Neuro Sciences (NIMHANS), Bengaluru, Karnataka, India., Menon RN; Cognition and Behavioral Neurology Section, Department of Neurology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, Kerala, India., Banerjee M; Human Molecular Genetics, Rajiv Gandhi Centre for Biotechnology, Trivandrum, Kerala, India.
Source:	Neurology India [Neurol India] 2026 Mar 01; Vol. 74 (2), pp. 277-281. Date of Electronic Publication: 2026 Mar 11.
Publication Type:	Journal Article; Case Reports
Journal Info:	Publisher: Medknow Publications Country of Publication: India NLM ID: 0042005 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1998-4022 (Electronic) Linking ISSN: 00283886 NLM ISO Abbreviation: Neurol India Subsets: MEDLINE
Database:	MEDLINE Ultimate

Description
ISSN:	1998-4022
DOI:	10.4103/neurol-india.Neurol-India-D-25-00391