Clinical and cellular features in patients with primary autosomal recessive microcephaly and a novel CDK5RAP2 mutation.
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| Title: | Clinical and cellular features in patients with primary autosomal recessive microcephaly and a novel CDK5RAP2 mutation. |
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| Authors: | Issa, Lina1,2, Mueller, Katrin3, Seufert, Katja3, Kraemer, Nadine1,2, Rosenkotter, Henning4, Ninnemann, Olaf1, Buob, Michael4, Kaindl, Angela M.1,2 angela.kaindl@charite.de, Morris-Rosendahl, Deborah J.3,5 deborah.morris-rosendahl@uniklinik-freiburg.de |
| Source: | Orphanet Journal of Rare Diseases. 2013, Vol. 8 Issue 1, Special section p1-14. 14p. 5 Color Photographs, 2 Black and White Photographs, 1 Chart. |
| Database: | Academic Search Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 87457647 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Clinical and cellular features in patients with primary autosomal recessive microcephaly and a novel CDK5RAP2 mutation. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Issa%2C+Lina%22">Issa, Lina</searchLink><relatesTo>1,2</relatesTo><br /><searchLink fieldCode="AR" term="%22Mueller%2C+Katrin%22">Mueller, Katrin</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Seufert%2C+Katja%22">Seufert, Katja</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Kraemer%2C+Nadine%22">Kraemer, Nadine</searchLink><relatesTo>1,2</relatesTo><br /><searchLink fieldCode="AR" term="%22Rosenkotter%2C+Henning%22">Rosenkotter, Henning</searchLink><relatesTo>4</relatesTo><br /><searchLink fieldCode="AR" term="%22Ninnemann%2C+Olaf%22">Ninnemann, Olaf</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Buob%2C+Michael%22">Buob, Michael</searchLink><relatesTo>4</relatesTo><br /><searchLink fieldCode="AR" term="%22Kaindl%2C+Angela+M%2E%22">Kaindl, Angela M.</searchLink><relatesTo>1,2</relatesTo><i> angela.kaindl@charite.de</i><br /><searchLink fieldCode="AR" term="%22Morris-Rosendahl%2C+Deborah+J%2E%22">Morris-Rosendahl, Deborah J.</searchLink><relatesTo>3,5</relatesTo><i> deborah.morris-rosendahl@uniklinik-freiburg.de</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Orphanet+Journal+of+Rare+Diseases%22">Orphanet Journal of Rare Diseases</searchLink>. 2013, Vol. 8 Issue 1, Special section p1-14. 14p. 5 Color Photographs, 2 Black and White Photographs, 1 Chart. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=87457647 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/1750-1172-8-59 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 14 StartPage: 1 Titles: – TitleFull: Clinical and cellular features in patients with primary autosomal recessive microcephaly and a novel CDK5RAP2 mutation. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Issa, Lina – PersonEntity: Name: NameFull: Mueller, Katrin – PersonEntity: Name: NameFull: Seufert, Katja – PersonEntity: Name: NameFull: Kraemer, Nadine – PersonEntity: Name: NameFull: Rosenkotter, Henning – PersonEntity: Name: NameFull: Ninnemann, Olaf – PersonEntity: Name: NameFull: Buob, Michael – PersonEntity: Name: NameFull: Kaindl, Angela M. – PersonEntity: Name: NameFull: Morris-Rosendahl, Deborah J. IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 05 Text: 2013 Type: published Y: 2013 Identifiers: – Type: issn-print Value: 17501172 Numbering: – Type: volume Value: 8 – Type: issue Value: 1 Titles: – TitleFull: Orphanet Journal of Rare Diseases Type: main |
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