Identification and functional interpretation of miRNAs affected by rare CNVs in CAKUT

Rare copy number variants (CNVs) are among the most common genomic disorders underlying CAKUT. miRNAs located in rare CNVs represent well-founded functional variants for human CAKUT research. The study aimed to identify and functionally interpret miRNAs most frequently affected by rare CNVs in CAKUT...

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Detalles Bibliográficos
Autores principales: Mitrovic, Kristina, Zivotic, Ivan, Kolic, Ivana, Djordjevic, Ana, Zakula, Jelena, Filipovic Trickovic, Jelena, Zivkovic, Maja, Stankovic, Aleksandra, Jovanovic, Ivan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9587983/
https://www.ncbi.nlm.nih.gov/pubmed/36273030
http://dx.doi.org/10.1038/s41598-022-22749-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9587983/
https://www.ncbi.nlm.nih.gov/pubmed/36273030
http://dx.doi.org/10.1038/s41598-022-22749-1

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