HECW2 Gene Mutation: A Rare Cause of West Syndrome: A Case Report.
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| Title: | HECW2 Gene Mutation: A Rare Cause of West Syndrome: A Case Report. |
|---|---|
| Authors: | Meena, Ankit Kumar1 (AUTHOR), Mahesan, Aakash1 (AUTHOR), Kamila, Gautam1 (AUTHOR), Jauhari, Prashant1 (AUTHOR), Chakrabarty, Biswaroop1 (AUTHOR), Kumar, Atin2 (AUTHOR), Gulati, Sheffali1 (AUTHOR) sheffaligulati@gmail.com |
| Source: | Neurology India. Jul/Aug2025, Vol. 73 Issue 4, p784-787. 4p. |
| Database: | Academic Search Ultimate |
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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 186887228 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: HECW2 Gene Mutation: A Rare Cause of West Syndrome: A Case Report. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Meena%2C+Ankit+Kumar%22">Meena, Ankit Kumar</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Mahesan%2C+Aakash%22">Mahesan, Aakash</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Kamila%2C+Gautam%22">Kamila, Gautam</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Jauhari%2C+Prashant%22">Jauhari, Prashant</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Chakrabarty%2C+Biswaroop%22">Chakrabarty, Biswaroop</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Kumar%2C+Atin%22">Kumar, Atin</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Gulati%2C+Sheffali%22">Gulati, Sheffali</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> sheffaligulati@gmail.com</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Neurology+India%22">Neurology India</searchLink>. Jul/Aug2025, Vol. 73 Issue 4, p784-787. 4p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=186887228 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.4103/neurol-india.Neurol-India-D-23-00203 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 4 StartPage: 784 Titles: – TitleFull: HECW2 Gene Mutation: A Rare Cause of West Syndrome: A Case Report. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Meena, Ankit Kumar – PersonEntity: Name: NameFull: Mahesan, Aakash – PersonEntity: Name: NameFull: Kamila, Gautam – PersonEntity: Name: NameFull: Jauhari, Prashant – PersonEntity: Name: NameFull: Chakrabarty, Biswaroop – PersonEntity: Name: NameFull: Kumar, Atin – PersonEntity: Name: NameFull: Gulati, Sheffali IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 07 Text: Jul/Aug2025 Type: published Y: 2025 Identifiers: – Type: issn-print Value: 00283886 Numbering: – Type: volume Value: 73 – Type: issue Value: 4 Titles: – TitleFull: Neurology India Type: main |
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