Myotonic dystrophy type 2 and modifier genes: an update on clinical and pathomolecular aspects
Myotonic dystrophy (DM) is the most common adult muscular dystrophy, characterized by
autosomal dominant progressive myopathy, myotonia, and multiorgan involvement. To date …
autosomal dominant progressive myopathy, myotonia, and multiorgan involvement. To date …
Myotonic dystrophy type 2 and modifier genes: an update on clinical and pathomolecular aspects.
G Meola, R Cardani - Neurological Sciences: Official Journal of the …, 2017 - europepmc.org
Myotonic dystrophy (DM) is the most common adult muscular dystrophy, characterized by
autosomal dominant progressive myopathy, myotonia, and multiorgan involvement. To date …
autosomal dominant progressive myopathy, myotonia, and multiorgan involvement. To date …
[PDF][PDF] Myotonic dystrophy type 2 and modifier genes: an update on clinical and pathomolecular aspects
G Meola, R Cardani - 2016 - researchgate.net
Myotonic dystrophy (DM) is the most common adult muscular dystrophy, characterized by
autosomal dominant progressive myopathy, myotonia, and multiorgan involvement. To date …
autosomal dominant progressive myopathy, myotonia, and multiorgan involvement. To date …
Myotonic dystrophy type 2 and modifier genes: an update on clinical and pathomolecular aspects
G Meola, R Cardani - Neurological Sciences, 2017 - search.proquest.com
Myotonic dystrophy (DM) is the most common adult muscular dystrophy, characterized by
autosomal dominant progressive myopathy, myotonia, and multiorgan involvement. To date …
autosomal dominant progressive myopathy, myotonia, and multiorgan involvement. To date …
Myotonic dystrophy type 2 and modifier genes: an update on clinical and pathomolecular aspects
G Meola, R Cardani - Neurological Sciences, 2017 - infona.pl
Myotonic dystrophy (DM) is the most common adult muscular dystrophy, characterized by
autosomal dominant progressive myopathy, myotonia, and multiorgan involvement. To date …
autosomal dominant progressive myopathy, myotonia, and multiorgan involvement. To date …
[引用][C] Myotonic dystrophy type 2 and modifier genes: an update on clinical and pathomolecular aspects
G Meola, R Cardani - Neurological Sciences, 2017 - cir.nii.ac.jp
Myotonic dystrophy type 2 and modifier genes: an update on clinical and pathomolecular
aspects | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細へ移動 検索 …
aspects | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細へ移動 検索 …
Myotonic dystrophy type 2 and modifier genes: an update on clinical and pathomolecular aspects
G Meola, R Cardani - NEUROLOGICAL SCIENCES, 2017 - air.unimi.it
Myotonic dystrophy (DM) is the most common adult muscular dystrophy, characterized by
autosomal dominant progressive myopathy, myotonia, and multiorgan involvement. To date …
autosomal dominant progressive myopathy, myotonia, and multiorgan involvement. To date …
Myotonic dystrophy type 2 and modifier genes: an update on clinical and pathomolecular aspects
G Meola, R Cardani - … Society and of the Italian Society of …, 2017 - pubmed.ncbi.nlm.nih.gov
Myotonic dystrophy (DM) is the most common adult muscular dystrophy, characterized by
autosomal dominant progressive myopathy, myotonia, and multiorgan involvement. To date …
autosomal dominant progressive myopathy, myotonia, and multiorgan involvement. To date …