Identification of novel MYO19 variants in neonatal hypertrophic cardiomyopathy: a familial analysis revealing oligogenic contributors to disease severity.
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| Title: | Identification of novel MYO19 variants in neonatal hypertrophic cardiomyopathy: a familial analysis revealing oligogenic contributors to disease severity. |
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| Authors: | Cho, Hye-Won1 (AUTHOR), Kim, Hyeseon2 (AUTHOR), Kim, Jeong-Min1 (AUTHOR), Shin, Dong Mun1 (AUTHOR), Kim, Oc-Hee1 (AUTHOR), Yang, Misun2,3 (AUTHOR), Jo, Heui Seung4 (AUTHOR), Jang, Mi-Ae5 (AUTHOR), Jang, Ja-Hyun5 (AUTHOR), Park, Hyun-Young6 (AUTHOR), Chang, Yun Sil2,3,7 (AUTHOR) yunsil.chang@gmail.com, Park, Mi-Hyun1 (AUTHOR) mihyun4868@korea.kr |
| Source: | Orphanet Journal of Rare Diseases. 7/9/2025, Vol. 20 Issue 1, p1-13. 13p. |
| Database: | Academic Search Ultimate |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 186488846 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Identification of novel MYO19 variants in neonatal hypertrophic cardiomyopathy: a familial analysis revealing oligogenic contributors to disease severity. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Cho%2C+Hye-Won%22">Cho, Hye-Won</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Kim%2C+Hyeseon%22">Kim, Hyeseon</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Kim%2C+Jeong-Min%22">Kim, Jeong-Min</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Shin%2C+Dong+Mun%22">Shin, Dong Mun</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Kim%2C+Oc-Hee%22">Kim, Oc-Hee</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Yang%2C+Misun%22">Yang, Misun</searchLink><relatesTo>2,3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Jo%2C+Heui+Seung%22">Jo, Heui Seung</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Jang%2C+Mi-Ae%22">Jang, Mi-Ae</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Jang%2C+Ja-Hyun%22">Jang, Ja-Hyun</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Park%2C+Hyun-Young%22">Park, Hyun-Young</searchLink><relatesTo>6</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Chang%2C+Yun+Sil%22">Chang, Yun Sil</searchLink><relatesTo>2,3,7</relatesTo> (AUTHOR)<i> yunsil.chang@gmail.com</i><br /><searchLink fieldCode="AR" term="%22Park%2C+Mi-Hyun%22">Park, Mi-Hyun</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> mihyun4868@korea.kr</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Orphanet+Journal+of+Rare+Diseases%22">Orphanet Journal of Rare Diseases</searchLink>. 7/9/2025, Vol. 20 Issue 1, p1-13. 13p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=186488846 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s13023-025-03871-5 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 13 StartPage: 1 Titles: – TitleFull: Identification of novel MYO19 variants in neonatal hypertrophic cardiomyopathy: a familial analysis revealing oligogenic contributors to disease severity. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Cho, Hye-Won – PersonEntity: Name: NameFull: Kim, Hyeseon – PersonEntity: Name: NameFull: Kim, Jeong-Min – PersonEntity: Name: NameFull: Shin, Dong Mun – PersonEntity: Name: NameFull: Kim, Oc-Hee – PersonEntity: Name: NameFull: Yang, Misun – PersonEntity: Name: NameFull: Jo, Heui Seung – PersonEntity: Name: NameFull: Jang, Mi-Ae – PersonEntity: Name: NameFull: Jang, Ja-Hyun – PersonEntity: Name: NameFull: Park, Hyun-Young – PersonEntity: Name: NameFull: Chang, Yun Sil – PersonEntity: Name: NameFull: Park, Mi-Hyun IsPartOfRelationships: – BibEntity: Dates: – D: 09 M: 07 Text: 7/9/2025 Type: published Y: 2025 Identifiers: – Type: issn-print Value: 17501172 Numbering: – Type: volume Value: 20 – Type: issue Value: 1 Titles: – TitleFull: Orphanet Journal of Rare Diseases Type: main |
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