Puzzling Out the Genetic Architecture of Endometriosis: Whole-Exome Sequencing and Novel Candidate Gene Identification in a Deeply Clinically Characterised Cohort

Endometriosis (EM) is a common multifactorial gynaecological disorder. Although Genome-Wide Association Studies have largely been employed, the current knowledge of the genetic mechanisms underlying EM is far from complete, and other approaches are needed. To this purpose, whole-exome sequencing (WE...

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Detalles Bibliográficos
Autores principales: Santin, Aurora, Spedicati, Beatrice, Morgan, Anna, Lenarduzzi, Stefania, Tesolin, Paola, Nardone, Giuseppe Giovanni, Mazzà, Daniela, Di Lorenzo, Giovanni, Romano, Federico, Buonomo, Francesca, Mangogna, Alessandro, Concas, Maria Pina, Zito, Gabriella, Ricci, Giuseppe, Girotto, Giorgia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10452899/
https://www.ncbi.nlm.nih.gov/pubmed/37626618
http://dx.doi.org/10.3390/biomedicines11082122

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10452899/
https://www.ncbi.nlm.nih.gov/pubmed/37626618
http://dx.doi.org/10.3390/biomedicines11082122

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