A homozygous mutation in SLC1A4 in siblings with severe intellectual disability and microcephaly.
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| Title: | A homozygous mutation in SLC1A4 in siblings with severe intellectual disability and microcephaly. |
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| Authors: | Srour, M.1,2, Hamdan, F. F.2, Gan‐Or, Z.3,4, Labuda, D.2,5, Nassif, C.2, Oskoui, M.1, Gana‐Weisz, M.6, Orr‐Urtreger, A.6,7, Rouleau, G.A.3,4,8, Michaud, J.L.2,5,9 |
| Source: | Clinical Genetics. Jul2015, Vol. 88 Issue 1, pE1-E4. 4p. |
| 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: 103105435 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=103105435 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1111/cge.12605 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 4 StartPage: E1 Titles: – TitleFull: A homozygous mutation in SLC1A4 in siblings with severe intellectual disability and microcephaly. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Srour, M. – PersonEntity: Name: NameFull: Hamdan, F. F. – PersonEntity: Name: NameFull: Gan‐Or, Z. – PersonEntity: Name: NameFull: Labuda, D. – PersonEntity: Name: NameFull: Nassif, C. – PersonEntity: Name: NameFull: Oskoui, M. – PersonEntity: Name: NameFull: Gana‐Weisz, M. – PersonEntity: Name: NameFull: Orr‐Urtreger, A. – PersonEntity: Name: NameFull: Rouleau, G.A. – PersonEntity: Name: NameFull: Michaud, J.L. IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 07 Text: Jul2015 Type: published Y: 2015 Identifiers: – Type: issn-print Value: 00099163 Numbering: – Type: volume Value: 88 – Type: issue Value: 1 Titles: – TitleFull: Clinical Genetics Type: main |
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