Nuclear envelope transmembrane proteins involved in genome organization are misregulated in myotonic dystrophy type 1 muscle

Myotonic dystrophy type 1 is a multisystemic disorder with predominant muscle and neurological involvement. Despite a well described pathomechanism, which is primarily a global missplicing due to sequestration of RNA-binding proteins, there are still many unsolved questions. One such question is the...

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Prif Awduron:	Vanessa Todorow, Stefan Hintze, Benedikt Schoser, Peter Meinke
Fformat:	Artigo
Iaith:	Inglês
Cyhoeddwyd:	Frontiers Media S.A. 2023-01-01
Cyfres:	Frontiers in Cell and Developmental Biology
Pynciau:	nuclear envelope myotonic dystrophy type 1 genome organization muscle biopsy nuclear envelope transmembrane proteins
Mynediad Ar-lein:	https://www.frontiersin.org/articles/10.3389/fcell.2022.1007331/full
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