A Heterozygous LMF1 Gene Mutation (c.1523C>T), Combined With an LPL Gene Mutation (c.590G>A), Aggravates the Clinical Symptoms in Hypertriglyceridemia

Hypertriglyceridemia is an important contributor to atherosclerotic cardiovascular disease (ASCVD) and acute pancreatitis. Familial hypertriglyceridemia is often caused by mutations in genes involved in triglyceride metabolism. Here, we investigated the disease-causing gene mutations in a Chinese fa...

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Detalles Bibliográficos
Autores principales: Guo, Danxia, Zheng, Yingchun, Gan, Zhongzhi, Guo, Yingying, Jiang, Sijie, Yang, Fang, Xiong, Fu, Zheng, Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8966663/
https://www.ncbi.nlm.nih.gov/pubmed/35368694
http://dx.doi.org/10.3389/fgene.2022.814295

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8966663/
https://www.ncbi.nlm.nih.gov/pubmed/35368694
http://dx.doi.org/10.3389/fgene.2022.814295

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