Clinical and Molecular Investigation of Familial Multiple Lipomatosis: Variants in the HMGA2 Gene

BACKGROUND: Familial multiple lipomatosis (FML) is an autosomal dominant disorder characterized by the slow growth of encapsulated nodules spread across the trunk and limbs. Currently, there is no specific etiology; therefore, its molecular and biological bases need to be better understood. High-thr...

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Detalles Bibliográficos
Autores principales: Mejía Granados, Diana Marcela, de Baptista, Marcella Bergamini, Bonadia, Luciana Cardoso, Bertuzzo, Carmen Silvia, Steiner, Carlos Eduardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6956394/
https://www.ncbi.nlm.nih.gov/pubmed/32021365
http://dx.doi.org/10.2147/CCID.S213139

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6956394/
https://www.ncbi.nlm.nih.gov/pubmed/32021365
http://dx.doi.org/10.2147/CCID.S213139

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