Novel homozygous nonsense mutation in the P5′N‐1 coding gene as an alternative cause for hereditary anemia with basophilic stippling.
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| Title: | Novel homozygous nonsense mutation in the P5′N‐1 coding gene as an alternative cause for hereditary anemia with basophilic stippling. |
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| Authors: | Kirschner, Martin1,2 (AUTHOR) mkirschner@ukaachen.de, Heinen, Inga Rebecca1,2 (AUTHOR), Koschmieder, Steffen1,2 (AUTHOR), Manco, Licinio3 (AUTHOR), Bento, Celeste4 (AUTHOR), Eggermann, Thomas5 (AUTHOR), Kurth, Ingo5 (AUTHOR), Jost, Edgar1,2 (AUTHOR), Brümmendorf, Tim H.1,2 (AUTHOR), Fuchs, Roland1,2 (AUTHOR) |
| Source: | Clinical Case Reports. Mar2022, Vol. 10 Issue 3, p1-6. 6p. |
| 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: 155950369 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Novel homozygous nonsense mutation in the P5′N‐1 coding gene as an alternative cause for hereditary anemia with basophilic stippling. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Kirschner%2C+Martin%22">Kirschner, Martin</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<i> mkirschner@ukaachen.de</i><br /><searchLink fieldCode="AR" term="%22Heinen%2C+Inga+Rebecca%22">Heinen, Inga Rebecca</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Koschmieder%2C+Steffen%22">Koschmieder, Steffen</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Manco%2C+Licinio%22">Manco, Licinio</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Bento%2C+Celeste%22">Bento, Celeste</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Eggermann%2C+Thomas%22">Eggermann, Thomas</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Kurth%2C+Ingo%22">Kurth, Ingo</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Jost%2C+Edgar%22">Jost, Edgar</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Brümmendorf%2C+Tim+H%2E%22">Brümmendorf, Tim H.</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Fuchs%2C+Roland%22">Fuchs, Roland</searchLink><relatesTo>1,2</relatesTo> (AUTHOR) – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Clinical+Case+Reports%22">Clinical Case Reports</searchLink>. Mar2022, Vol. 10 Issue 3, p1-6. 6p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=155950369 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/ccr3.5501 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 6 StartPage: 1 Titles: – TitleFull: Novel homozygous nonsense mutation in the P5′N‐1 coding gene as an alternative cause for hereditary anemia with basophilic stippling. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Kirschner, Martin – PersonEntity: Name: NameFull: Heinen, Inga Rebecca – PersonEntity: Name: NameFull: Koschmieder, Steffen – PersonEntity: Name: NameFull: Manco, Licinio – PersonEntity: Name: NameFull: Bento, Celeste – PersonEntity: Name: NameFull: Eggermann, Thomas – PersonEntity: Name: NameFull: Kurth, Ingo – PersonEntity: Name: NameFull: Jost, Edgar – PersonEntity: Name: NameFull: Brümmendorf, Tim H. – PersonEntity: Name: NameFull: Fuchs, Roland IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 03 Text: Mar2022 Type: published Y: 2022 Identifiers: – Type: issn-print Value: 20500904 Numbering: – Type: volume Value: 10 – Type: issue Value: 3 Titles: – TitleFull: Clinical Case Reports Type: main |
| ResultId | 1 |