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 years
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/1497915
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