Establishing the Mutational Spectrum of Hungarian Patients with Familial Hypercholesterolemia

Familial hypercholesterolemia (FH) is one of the most common autosomal, dominantly inherited diseases affecting cholesterol metabolism, which, in the absence of treatment, leads to the development of cardiovascular complications. The disease is still underdiagnosed, even though an early diagnosis wo...

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Detalles Bibliográficos
Autores principales: Madar, László, Juhász, Lilla, Szűcs, Zsuzsanna, Kerkovits, Lóránt, Harangi, Mariann, Balogh, István
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8775528/
https://www.ncbi.nlm.nih.gov/pubmed/35052492
http://dx.doi.org/10.3390/genes13010153

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8775528/
https://www.ncbi.nlm.nih.gov/pubmed/35052492
http://dx.doi.org/10.3390/genes13010153

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