Genomic and epigenomic techniques identify a new variation type causing Mendelian disease by altering the non-coding regulatory network in thyroid cells — solving a hidden cause linked for 20 years
Contraction or sequence variant of an intergenic repeat-Alu element leads to inherited thyroid disease
Cortese, Andrea;
2024-01-01
Abstract
Genomic and epigenomic techniques identify a new variation type causing Mendelian disease by altering the non-coding regulatory network in thyroid cells — solving a hidden cause linked for 20 yearsFile in questo prodotto:
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