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Screening program for familial hyperchylomicronemia syndrome detection: Experience of a university health system
OBJECTIVE: Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive metabolic disorder caused by mutations related to chylomicron metabolism. The objective of this study is to show the development and results of a screening program for FCS in Argentina. MATERIALS AND METHODS: A cross-se...
Autores principales: | Masson, Walter, Barbagelata, Leandro, Fleitas, Milagros, Herzkovich, Nicole, Kerschner, Eliana, Rossi, Emiliano, Siniawski, Daniel, Ami, María V., Nogueira, Juan P. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Endocrinologia e Metabologia
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10247249/ https://www.ncbi.nlm.nih.gov/pubmed/36748937 http://dx.doi.org/10.20945/2359-3997000000601 |
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