Short tandem repeat expansions in LRP12 are absent in cohorts of familial and sporadic amyotrophic lateral sclerosis patients of European ancestry.
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| Title: | Short tandem repeat expansions in LRP12 are absent in cohorts of familial and sporadic amyotrophic lateral sclerosis patients of European ancestry. |
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| Authors: | Henden, Lyndal1 (AUTHOR), Fearnley, Liam G.2,3 (AUTHOR), Southwood, Dean1 (AUTHOR), Smith, Andrew1 (AUTHOR), Rowe, Dominic B.1 (AUTHOR), Kiernan, Matthew C.4,5 (AUTHOR), Pamphlett, Roger4,6,7 (AUTHOR), Bahlo, Melanie2,3 (AUTHOR), Blair, Ian P.1 (AUTHOR), Williams, Kelly L.1 (AUTHOR) kelly.williams@mq.edu.au |
| Source: | Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. Aug2024, Vol. 25 Issue 5/6, p644-647. 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: 178651570 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Short tandem repeat expansions in LRP12 are absent in cohorts of familial and sporadic amyotrophic lateral sclerosis patients of European ancestry. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Henden%2C+Lyndal%22">Henden, Lyndal</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Fearnley%2C+Liam+G%2E%22">Fearnley, Liam G.</searchLink><relatesTo>2,3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Southwood%2C+Dean%22">Southwood, Dean</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Smith%2C+Andrew%22">Smith, Andrew</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Rowe%2C+Dominic+B%2E%22">Rowe, Dominic B.</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Kiernan%2C+Matthew+C%2E%22">Kiernan, Matthew C.</searchLink><relatesTo>4,5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Pamphlett%2C+Roger%22">Pamphlett, Roger</searchLink><relatesTo>4,6,7</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Bahlo%2C+Melanie%22">Bahlo, Melanie</searchLink><relatesTo>2,3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Blair%2C+Ian+P%2E%22">Blair, Ian P.</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Williams%2C+Kelly+L%2E%22">Williams, Kelly L.</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> kelly.williams@mq.edu.au</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Amyotrophic+Lateral+Sclerosis+%26+Frontotemporal+Degeneration%22">Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration</searchLink>. Aug2024, Vol. 25 Issue 5/6, p644-647. 4p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=178651570 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1080/21678421.2024.2348636 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 4 StartPage: 644 Titles: – TitleFull: Short tandem repeat expansions in LRP12 are absent in cohorts of familial and sporadic amyotrophic lateral sclerosis patients of European ancestry. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Henden, Lyndal – PersonEntity: Name: NameFull: Fearnley, Liam G. – PersonEntity: Name: NameFull: Southwood, Dean – PersonEntity: Name: NameFull: Smith, Andrew – PersonEntity: Name: NameFull: Rowe, Dominic B. – PersonEntity: Name: NameFull: Kiernan, Matthew C. – PersonEntity: Name: NameFull: Pamphlett, Roger – PersonEntity: Name: NameFull: Bahlo, Melanie – PersonEntity: Name: NameFull: Blair, Ian P. – PersonEntity: Name: NameFull: Williams, Kelly L. IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 08 Text: Aug2024 Type: published Y: 2024 Identifiers: – Type: issn-print Value: 21678421 Numbering: – Type: volume Value: 25 – Type: issue Value: 5/6 Titles: – TitleFull: Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration Type: main |
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