LCAT deficiency: a systematic review with the clinical and genetic description of Mexican kindred

BACKGROUND: LCAT (lecithin-cholesterol acyltransferase) deficiency is characterized by two distinct phenotypes, familial LCAT deficiency (FLD) and Fish Eye disease (FED). This is the first systematic review evaluating the ethnic distribution of LCAT deficiency, with particular emphasis on Latin Amer...

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Detalles Bibliográficos
Autores principales: Mehta, Roopa, Elías-López, Daniel, Martagón, Alexandro J., Pérez-Méndez, Oscar A, Sánchez, Maria Luisa Ordóñez, Segura, Yayoi, Tusié, Maria Teresa, Aguilar-Salinas, Carlos A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8276382/
https://www.ncbi.nlm.nih.gov/pubmed/34256778
http://dx.doi.org/10.1186/s12944-021-01498-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8276382/
https://www.ncbi.nlm.nih.gov/pubmed/34256778
http://dx.doi.org/10.1186/s12944-021-01498-6

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