Describing the First Canadian Cohort of Oculogastrointestinal Neurodevelopmental Syndrome Caused by CAPN15 Pathogenic Variants.
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| Title: | Describing the First Canadian Cohort of Oculogastrointestinal Neurodevelopmental Syndrome Caused by CAPN15 Pathogenic Variants. |
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| Authors: | Lin, Eric1, Cruz‐Marino, Tania2, Chrestian, Nicolas3, Leblanc, Josianne4, Rioux, Nadie5, Labrie, Yvan5, Rivest, Serge5, Lace, Baiba5,6, Colaiacovo, Samantha1,7, Saleh, Maha1,7, maha.saleh@lhsc.on.ca |
| Source: | American Journal of Medical Genetics. Part A; Oct2025, Vol. 197 Issue 10, p1-7, 7p |
| Database: | Applied Science & Technology Source |
| FullText | Text: Availability: 0 |
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| Header | DbId: aci DbLabel: Applied Science & Technology Source An: 187859778 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=aci&AN=187859778 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/ajmg.a.64133 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 7 StartPage: 1 Titles: – TitleFull: Describing the First Canadian Cohort of Oculogastrointestinal Neurodevelopmental Syndrome Caused by CAPN15 Pathogenic Variants. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Lin, Eric – PersonEntity: Name: NameFull: Cruz‐Marino, Tania – PersonEntity: Name: NameFull: Chrestian, Nicolas – PersonEntity: Name: NameFull: Leblanc, Josianne – PersonEntity: Name: NameFull: Rioux, Nadie – PersonEntity: Name: NameFull: Labrie, Yvan – PersonEntity: Name: NameFull: Rivest, Serge – PersonEntity: Name: NameFull: Lace, Baiba – PersonEntity: Name: NameFull: Colaiacovo, Samantha – PersonEntity: Name: NameFull: Saleh, Maha IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 10 Text: Oct2025 Type: published Y: 2025 Identifiers: – Type: issn-print Value: 15524825 Numbering: – Type: volume Value: 197 – Type: issue Value: 10 Titles: – TitleFull: American Journal of Medical Genetics. Part A Type: main |
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