Molecular autopsy and family screening in a young case of sudden cardiac death reveals an unusually severe case of FHL1 related hypertrophic cardiomyopathy

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Molecular autopsy and family screening in a young case of sudden cardiac death reveals an unusually severe case of FHL1 related hypertrophic cardiomyopathy

Dades bibliogràfiques
Publicat a:	Molecular genetics & genomic medicine 7(2019)8, S. e841
Autors principals:	Gaertner-Rommel, Anna (Autor), Tiesmeier, Jens (Autor), Jacob, Thomas (Autor)
Format:	Article
Idioma:	English
Publicat:	2019
Matèries:	Publikation <Klinikum Herford> Anästhesiologie <Universitätsklinik, Klinikum Herford> Klinikum Herford Zeitschriftenartikel
Accés en línia:	https://doi.org/10.1002/mgg3.841
Publicació relacionada:	In: Molecular genetics & genomic medicine

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