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Clinical, biochemical and molecular analysis of two infants with familial chylomicronemia syndrome

Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive disease due mainly to inherited deficiencies in the proteins or enzymes involved in the clearance of triglycerides from circulation. It usually happens in late childhood and adolescence, which can have serious consequences if misd...

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Detalhes bibliográficos
Publicado no:Lipids Health Dis
Main Authors: Zhang, Yonghong, Zhou, Jing, Zheng, Wenxin, Lan, Zhangzhang, Huang, Zhiwei, Yang, Qingnan, Liu, Chengbo, Gao, Rui, Zhang, Yongjun
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2016
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4859971/
https://ncbi.nlm.nih.gov/pubmed/27153815
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12944-016-0254-z
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