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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| ISSN: | 17501172 |
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| DOI: | 10.1186/s13023-025-03871-5 |
