Edgetic Perturbations Contribute to Phenotypic Variability in PEX26 Deficiency.
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| Title: | Edgetic Perturbations Contribute to Phenotypic Variability in PEX26 Deficiency. |
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| Authors: | Lotz-Havla AS; Dr. von Hauner Children's Hospital, Ludwig-Maximilians-University, Munich, Germany., Woidy M; University Children's Research, University Medical Center Hamburg-Eppendorf, Hamburg, Germany., Guder P; University Children's Research, University Medical Center Hamburg-Eppendorf, Hamburg, Germany., Schmiesing J; University Children's Research, University Medical Center Hamburg-Eppendorf, Hamburg, Germany., Erdmann R; Institut für Physiologische Chemie, Medizinische Fakultät der Ruhr-Universität Bochum, Bochum, Germany., Waterham HR; Laboratory Genetic Metabolic Diseases, Academic Medical Center, University of Amsterdam, Amsterdam, Netherlands., Muntau AC; Children's Hospital, University Medical Center Hamburg-Eppendorf, Hamburg, Germany., Gersting SW; University Children's Research, University Medical Center Hamburg-Eppendorf, Hamburg, Germany. |
| Source: | Frontiers in genetics [Front Genet] 2021 Nov 04; Vol. 12, pp. 726174. Date of Electronic Publication: 2021 Nov 04 (Print Publication: 2021). |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101560621 Publication Model: eCollection Cited Medium: Print ISSN: 1664-8021 (Print) Linking ISSN: 16648021 NLM ISO Abbreviation: Front Genet Subsets: PubMed not MEDLINE |
| Database: | MEDLINE Ultimate |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 34804114 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Edgetic Perturbations Contribute to Phenotypic Variability in PEX26 Deficiency. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Lotz-Havla+AS%22">Lotz-Havla AS</searchLink>; Dr. von Hauner Children's Hospital, Ludwig-Maximilians-University, Munich, Germany.<br /><searchLink fieldCode="AU" term="%22Woidy+M%22">Woidy M</searchLink>; University Children's Research, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.<br /><searchLink fieldCode="AU" term="%22Guder+P%22">Guder P</searchLink>; University Children's Research, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.<br /><searchLink fieldCode="AU" term="%22Schmiesing+J%22">Schmiesing J</searchLink>; University Children's Research, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.<br /><searchLink fieldCode="AU" term="%22Erdmann+R%22">Erdmann R</searchLink>; Institut für Physiologische Chemie, Medizinische Fakultät der Ruhr-Universität Bochum, Bochum, Germany.<br /><searchLink fieldCode="AU" term="%22Waterham+HR%22">Waterham HR</searchLink>; Laboratory Genetic Metabolic Diseases, Academic Medical Center, University of Amsterdam, Amsterdam, Netherlands.<br /><searchLink fieldCode="AU" term="%22Muntau+AC%22">Muntau AC</searchLink>; Children's Hospital, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.<br /><searchLink fieldCode="AU" term="%22Gersting+SW%22">Gersting SW</searchLink>; University Children's Research, University Medical Center Hamburg-Eppendorf, Hamburg, Germany. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101560621%22">Frontiers in genetics</searchLink> [Front Genet] 2021 Nov 04; Vol. 12, pp. 726174. <i>Date of Electronic Publication: </i>2021 Nov 04 (<i>Print Publication: </i>2021). – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Frontiers+Research+Foundation%22">Frontiers Research Foundation </searchLink><i>Country of Publication: </i>Switzerland <i>NLM ID: </i>101560621 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Print <i>ISSN: </i>1664-8021 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2216648021%22">16648021 </searchLink><i>NLM ISO Abbreviation: </i>Front Genet <i>Subsets: </i>PubMed not MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=34804114 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.3389/fgene.2021.726174 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 726174 Titles: – TitleFull: Edgetic Perturbations Contribute to Phenotypic Variability in PEX26 Deficiency. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Lotz-Havla AS – PersonEntity: Name: NameFull: Woidy M – PersonEntity: Name: NameFull: Guder P – PersonEntity: Name: NameFull: Schmiesing J – PersonEntity: Name: NameFull: Erdmann R – PersonEntity: Name: NameFull: Waterham HR – PersonEntity: Name: NameFull: Muntau AC – PersonEntity: Name: NameFull: Gersting SW IsPartOfRelationships: – BibEntity: Dates: – D: 04 M: 11 Text: 2021 Nov 04 Type: published Y: 2021 Identifiers: – Type: issn-print Value: 1664-8021 Numbering: – Type: volume Value: 12 Titles: – TitleFull: Frontiers in genetics Type: main |
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