Current studies concerning myotonic dystrophy type 1 (DM1) are in the process of transitioning from molecular investigations to preclinical and clinical trials [...
Type 1 myotonic dystrophy or DM1 (Steinert's disease), which is the commonest muscular dystrophy in ...
Myotonic dystrophy type 1 (DM1 also known as Steinert disease) is a multisystemic disorder mainly ch...
Contains fulltext : 91254.pdf (publisher's version ) (Open Access)Radboud Universi...
International audienceMyotonic dystrophies are multisystemic diseases characterized not only by musc...
Myotonic dystrophy type 1 (DM1) is the most common muscular dystrophy affecting many different body ...
Omics studies are crucial to improve our understanding of myotonic dystrophy type 1 (DM1), the most ...
Myotonic dystrophy (DM) is the most common adult muscular dystrophy, characterized by autosomal domi...
New discoveries showing the key role of RNAs in diseases such as cancer and neurodegenerative disord...
Myotonic Dystrophy type 1 (DM1) is a genetic disorder caused by an expansion of a (CTG)n repeat in t...
There are currently two clinically and molecularly defined forms of myotonic dystrophy: (1) myotonic...
Myotonic dystrophy type 1 (DM1) is a progressive multisystemic disease caused by the expansion of a ...
Myotonic dystrophy type 1 (DM1) is the most common muscular dystrophy that affects multiple systems ...
AbstractMyotonic dystrophy (DM) is the most common adult muscular dystrophy, characterized by autoso...
Contains fulltext : mmubn000001_132009447.pdf (publisher's version ) (Open Access)...
Contains fulltext : 89133.pdf (publisher's version ) (Closed access)Myotonic dystr...
Type 1 myotonic dystrophy or DM1 (Steinert's disease), which is the commonest muscular dystrophy in ...
Myotonic dystrophy type 1 (DM1 also known as Steinert disease) is a multisystemic disorder mainly ch...
Contains fulltext : 91254.pdf (publisher's version ) (Open Access)Radboud Universi...
International audienceMyotonic dystrophies are multisystemic diseases characterized not only by musc...
Myotonic dystrophy type 1 (DM1) is the most common muscular dystrophy affecting many different body ...
Omics studies are crucial to improve our understanding of myotonic dystrophy type 1 (DM1), the most ...
Myotonic dystrophy (DM) is the most common adult muscular dystrophy, characterized by autosomal domi...
New discoveries showing the key role of RNAs in diseases such as cancer and neurodegenerative disord...
Myotonic Dystrophy type 1 (DM1) is a genetic disorder caused by an expansion of a (CTG)n repeat in t...
There are currently two clinically and molecularly defined forms of myotonic dystrophy: (1) myotonic...
Myotonic dystrophy type 1 (DM1) is a progressive multisystemic disease caused by the expansion of a ...
Myotonic dystrophy type 1 (DM1) is the most common muscular dystrophy that affects multiple systems ...
AbstractMyotonic dystrophy (DM) is the most common adult muscular dystrophy, characterized by autoso...
Contains fulltext : mmubn000001_132009447.pdf (publisher's version ) (Open Access)...
Contains fulltext : 89133.pdf (publisher's version ) (Closed access)Myotonic dystr...
Type 1 myotonic dystrophy or DM1 (Steinert's disease), which is the commonest muscular dystrophy in ...
Myotonic dystrophy type 1 (DM1 also known as Steinert disease) is a multisystemic disorder mainly ch...
Contains fulltext : 91254.pdf (publisher's version ) (Open Access)Radboud Universi...
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