Investigators at Newcastle University, UK, and Hopitaux de Paris, France, report 5 patients from 3 unrelated families with a strikingly homogeneous clinical entity combining congenital myasthenia with distal muscle weakness and atrophy resembling a distal myopathy
Congenital myasthenic syndromes are clinically and genetically heterogeneous disorders of neuromuscu...
International audienceCongenital myasthenic syndromes (CMS) form a heterogeneous group of rare disea...
Congenital myasthenic syndromes are clinically and genetically heterogeneous disorders of neuromuscu...
International audienceCongenital myasthenic syndromes are a clinically and genetically heterogeneous...
The congenital myasthenic syndromes (CMS) are rare inherited disorders of neuromuscular transmission...
BACKGROUND: A newly defined congenital myasthenic syndrome (CMS) caused by DPAGT1 mutations has rece...
© 2022 Elsevier Inc.Background: Congenital myasthenic syndromes (CMS) are composed of numerous hered...
Background A newly defined congenital myasthenic syndrome (CMS) caused by DPAGT1 mutations has recen...
he congenital myasthenic syndromes (CMS) are a heterogeneous group of inherited disorders affect-ing...
ABSTRACT Neuromuscular junction disorders represent a wide group of neurological diseases characteri...
Congenital myasthenic syndromes are a rare group of heterogeneous disorders affecting neuromuscular ...
Mutations in DPAGT1 are a newly recognised cause of congenital myasthenic syndrome. DPAGT1 encodes a...
Abstract Objective We aimed to summarize the clinical, genetic, and myopathological features of a co...
AbstractMutations in DPAGT1 are a newly recognised cause of congenital myasthenic syndrome. DPAGT1 e...
International audienceCongenital myasthenic syndromes (CMS) are a clinically and genetically heterog...
Congenital myasthenic syndromes are clinically and genetically heterogeneous disorders of neuromuscu...
International audienceCongenital myasthenic syndromes (CMS) form a heterogeneous group of rare disea...
Congenital myasthenic syndromes are clinically and genetically heterogeneous disorders of neuromuscu...
International audienceCongenital myasthenic syndromes are a clinically and genetically heterogeneous...
The congenital myasthenic syndromes (CMS) are rare inherited disorders of neuromuscular transmission...
BACKGROUND: A newly defined congenital myasthenic syndrome (CMS) caused by DPAGT1 mutations has rece...
© 2022 Elsevier Inc.Background: Congenital myasthenic syndromes (CMS) are composed of numerous hered...
Background A newly defined congenital myasthenic syndrome (CMS) caused by DPAGT1 mutations has recen...
he congenital myasthenic syndromes (CMS) are a heterogeneous group of inherited disorders affect-ing...
ABSTRACT Neuromuscular junction disorders represent a wide group of neurological diseases characteri...
Congenital myasthenic syndromes are a rare group of heterogeneous disorders affecting neuromuscular ...
Mutations in DPAGT1 are a newly recognised cause of congenital myasthenic syndrome. DPAGT1 encodes a...
Abstract Objective We aimed to summarize the clinical, genetic, and myopathological features of a co...
AbstractMutations in DPAGT1 are a newly recognised cause of congenital myasthenic syndrome. DPAGT1 e...
International audienceCongenital myasthenic syndromes (CMS) are a clinically and genetically heterog...
Congenital myasthenic syndromes are clinically and genetically heterogeneous disorders of neuromuscu...
International audienceCongenital myasthenic syndromes (CMS) form a heterogeneous group of rare disea...
Congenital myasthenic syndromes are clinically and genetically heterogeneous disorders of neuromuscu...