A Novel Rare Homozygous R47C Variant in TREM2 with Frontal Variant Alzheimer's Disease.
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| Title: | A Novel Rare Homozygous R47C Variant in TREM2 with Frontal Variant Alzheimer's Disease. |
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| 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 |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 41817071 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: A Novel Rare Homozygous R47C Variant in TREM2 with Frontal Variant Alzheimer's Disease. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Mallika+AP%22">Mallika AP</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Mathuranath+PS%22">Mathuranath PS</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Menon+RN%22">Menon RN</searchLink>; Cognition and Behavioral Neurology Section, Department of Neurology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, Kerala, India.<br /><searchLink fieldCode="AU" term="%22Banerjee+M%22">Banerjee M</searchLink>; Human Molecular Genetics, Rajiv Gandhi Centre for Biotechnology, Trivandrum, Kerala, India. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%220042005%22">Neurology India</searchLink> [Neurol India] 2026 Mar 01; Vol. 74 (2), pp. 277-281. <i>Date of Electronic Publication: </i>2026 Mar 11. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Case Reports – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Medknow+Publications%22">Medknow Publications </searchLink><i>Country of Publication: </i>India <i>NLM ID: </i>0042005 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1998-4022 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200283886%22">00283886 </searchLink><i>NLM ISO Abbreviation: </i>Neurol India <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=41817071 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.4103/neurol-india.Neurol-India-D-25-00391 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 277 Titles: – TitleFull: A Novel Rare Homozygous R47C Variant in TREM2 with Frontal Variant Alzheimer's Disease. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Mallika AP – PersonEntity: Name: NameFull: Mathuranath PS – PersonEntity: Name: NameFull: Menon RN – PersonEntity: Name: NameFull: Banerjee M IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 03 Text: 2026 Mar 01 Type: published Y: 2026 Identifiers: – Type: issn-electronic Value: 1998-4022 Numbering: – Type: volume Value: 74 – Type: issue Value: 2 Titles: – TitleFull: Neurology India Type: main |
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