Oculopharyngeal muscular dystrophy: a polyalanine myopathy
B Brais - Current neurology and neuroscience reports, 2009 - Springer
It has been 10 years since the identification of the first PABPN1 gene (GCN) n/polyalanine
mutations responsible for oculopharyngeal muscular dystrophy (OPMD). These mutations …
mutations responsible for oculopharyngeal muscular dystrophy (OPMD). These mutations …
Oculopharyngeal muscular dystrophy: A polyalanine myopathy
B Brais - Current Neurology and Neuroscience Reports, 2009 - search.proquest.com
It has been 10 years since the identification of the first PABPN1 gene (GCN)^ sub
n^/polyalanine mutations responsible for oculopharyngeal muscular dystrophy (OPMD) …
n^/polyalanine mutations responsible for oculopharyngeal muscular dystrophy (OPMD) …
Oculopharyngeal muscular dystrophy: a polyalanine myopathy
B Brais - Current neurology and neuroscience reports, 2009 - pubmed.ncbi.nlm.nih.gov
It has been 10 years since the identification of the first PABPN1 gene (GCN)(n)/polyalanine
mutations responsible for oculopharyngeal muscular dystrophy (OPMD). These mutations …
mutations responsible for oculopharyngeal muscular dystrophy (OPMD). These mutations …
Oculopharyngeal muscular dystrophy: A polyalanine myopathy
B Brais - Current Neurology and Neuroscience Reports, 2009 - infona.pl
It has been 10 years since the identification of the first PABPN1 gene (GCN) n/polyalanine
mutations responsible for oculopharyngeal muscular dystrophy (OPMD). These mutations …
mutations responsible for oculopharyngeal muscular dystrophy (OPMD). These mutations …
Oculopharyngeal muscular dystrophy: a polyalanine myopathy.
B Brais - Current Neurology and Neuroscience Reports, 2009 - europepmc.org
It has been 10 years since the identification of the first PABPN1 gene (GCN)(n)/polyalanine
mutations responsible for oculopharyngeal muscular dystrophy (OPMD). These mutations …
mutations responsible for oculopharyngeal muscular dystrophy (OPMD). These mutations …