Recurrent mutations in DNAJC5 cause autosomal dominant Kufs disease.
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| Title: | Recurrent mutations in DNAJC5 cause autosomal dominant Kufs disease. |
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| Authors: | Cadieux‐Dion, M1, Andermann, E2, Lachance‐Touchette, P1, Ansorge, O3, Meloche, C1, Barnabé, A2, Kuzniecky, RI4, Andermann, F2, Faught, E5, Leonberg, S6, Damiano, JA7, Berkovic, SF7, Rouleau, GA1, Cossette, P1 |
| Source: | Clinical Genetics. Jun2013, Vol. 83 Issue 6, p571-575. 5p. 1 Diagram, 1 Chart, 1 Graph. |
| Database: | Academic Search Ultimate |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 87106349 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=87106349 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1111/cge.12020 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 5 StartPage: 571 Titles: – TitleFull: Recurrent mutations in DNAJC5 cause autosomal dominant Kufs disease. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Cadieux‐Dion, M – PersonEntity: Name: NameFull: Andermann, E – PersonEntity: Name: NameFull: Lachance‐Touchette, P – PersonEntity: Name: NameFull: Ansorge, O – PersonEntity: Name: NameFull: Meloche, C – PersonEntity: Name: NameFull: Barnabé, A – PersonEntity: Name: NameFull: Kuzniecky, RI – PersonEntity: Name: NameFull: Andermann, F – PersonEntity: Name: NameFull: Faught, E – PersonEntity: Name: NameFull: Leonberg, S – PersonEntity: Name: NameFull: Damiano, JA – PersonEntity: Name: NameFull: Berkovic, SF – PersonEntity: Name: NameFull: Rouleau, GA – PersonEntity: Name: NameFull: Cossette, P IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 06 Text: Jun2013 Type: published Y: 2013 Identifiers: – Type: issn-print Value: 00099163 Numbering: – Type: volume Value: 83 – Type: issue Value: 6 Titles: – TitleFull: Clinical Genetics Type: main |
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