GLRX5-associated [Fe-S] cluster biogenesis disorder: further characterisation of the neurological phenotype and long-term outcome.
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| Title: | GLRX5-associated [Fe-S] cluster biogenesis disorder: further characterisation of the neurological phenotype and long-term outcome. |
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| Authors: | Sankaran, Bindu Parayil1,2 (AUTHOR), Gupta, Sachin2,3 (AUTHOR), Tchan, Michel4 (AUTHOR), Devanapalli, Beena1 (AUTHOR), Rahman, Yusof4 (AUTHOR), Procopis, Peter2,3 (AUTHOR), Bhattacharya, Kaustuv1,2 (AUTHOR) Kaustuv.bhattacharya@health.nsw.gov.au |
| Source: | Orphanet Journal of Rare Diseases. 11/3/2021, Vol. 16 Issue 1, p1-12. 12p. |
| 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: 153414332 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: GLRX5-associated [Fe-S] cluster biogenesis disorder: further characterisation of the neurological phenotype and long-term outcome. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Sankaran%2C+Bindu+Parayil%22">Sankaran, Bindu Parayil</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Gupta%2C+Sachin%22">Gupta, Sachin</searchLink><relatesTo>2,3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Tchan%2C+Michel%22">Tchan, Michel</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Devanapalli%2C+Beena%22">Devanapalli, Beena</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Rahman%2C+Yusof%22">Rahman, Yusof</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Procopis%2C+Peter%22">Procopis, Peter</searchLink><relatesTo>2,3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Bhattacharya%2C+Kaustuv%22">Bhattacharya, Kaustuv</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<i> Kaustuv.bhattacharya@health.nsw.gov.au</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Orphanet+Journal+of+Rare+Diseases%22">Orphanet Journal of Rare Diseases</searchLink>. 11/3/2021, Vol. 16 Issue 1, p1-12. 12p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=153414332 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s13023-021-02073-z Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 12 StartPage: 1 Titles: – TitleFull: GLRX5-associated [Fe-S] cluster biogenesis disorder: further characterisation of the neurological phenotype and long-term outcome. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Sankaran, Bindu Parayil – PersonEntity: Name: NameFull: Gupta, Sachin – PersonEntity: Name: NameFull: Tchan, Michel – PersonEntity: Name: NameFull: Devanapalli, Beena – PersonEntity: Name: NameFull: Rahman, Yusof – PersonEntity: Name: NameFull: Procopis, Peter – PersonEntity: Name: NameFull: Bhattacharya, Kaustuv IsPartOfRelationships: – BibEntity: Dates: – D: 03 M: 11 Text: 11/3/2021 Type: published Y: 2021 Identifiers: – Type: issn-print Value: 17501172 Numbering: – Type: volume Value: 16 – Type: issue Value: 1 Titles: – TitleFull: Orphanet Journal of Rare Diseases Type: main |
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