Molecular autopsy and family screening in a young case of sudden cardiac death reveals an unusually severe case of FHL1 related hypertrophic cardiomyopathy
Yayımlandı: | Molecular genetics & genomic medicine 7(2019)8, S. e841 |
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Asıl Yazarlar: | Gaertner-Rommel, Anna (Yazar), Tiesmeier, Jens (Yazar), Jacob, Thomas (Yazar) |
Materyal Türü: | Makale |
Dil: | English |
Baskı/Yayın Bilgisi: |
2019
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Konular: | |
Online Erişim: | https://doi.org/10.1002/mgg3.841 |
İlgili Kayıtlar: | In:
Molecular genetics & genomic medicine |
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