A novel DHTKD1 gene mutation with ALS like presentation: a case report.
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| Title: | A novel DHTKD1 gene mutation with ALS like presentation: a case report. |
|---|---|
| Authors: | Menon, Deepak1 (AUTHOR), Nashi, Saraswati1 (AUTHOR), Mohanty, Manisha1 (AUTHOR), Dubbal, Rohin1 (AUTHOR), MK, Farsana1 (AUTHOR), Vengalil, Seena1 (AUTHOR), Thomas, Aneesha1 (AUTHOR), Kumar, Vijay1 (AUTHOR), Baskar, Dipti1 (AUTHOR), Arunachal, Gautham2 (AUTHOR), Nalini, Atchayaram1 (AUTHOR) atchayaramnalini@yahoo.co.in |
| Source: | Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. May2024, Vol. 25 Issue 3/4, p413-415. 3p. |
| Database: | Academic Search Ultimate |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 176695471 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=176695471 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1080/21678421.2023.2273366 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 3 StartPage: 413 Titles: – TitleFull: A novel DHTKD1 gene mutation with ALS like presentation: a case report. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Menon, Deepak – PersonEntity: Name: NameFull: Nashi, Saraswati – PersonEntity: Name: NameFull: Mohanty, Manisha – PersonEntity: Name: NameFull: Dubbal, Rohin – PersonEntity: Name: NameFull: MK, Farsana – PersonEntity: Name: NameFull: Vengalil, Seena – PersonEntity: Name: NameFull: Thomas, Aneesha – PersonEntity: Name: NameFull: Kumar, Vijay – PersonEntity: Name: NameFull: Baskar, Dipti – PersonEntity: Name: NameFull: Arunachal, Gautham – PersonEntity: Name: NameFull: Nalini, Atchayaram IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 05 Text: May2024 Type: published Y: 2024 Identifiers: – Type: issn-print Value: 21678421 Numbering: – Type: volume Value: 25 – Type: issue Value: 3/4 Titles: – TitleFull: Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration Type: main |
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