Add to ORKGProximal spinal muscular atrophy (SMA) is one of the most common autosomal recessive disorders. It is characterised by degeneration of the anterior horn cells of the spinal cord, resulting in symmetrical limb muscl
Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disease characterized by regen...
Spinal muscular atrophy (SMA) is autosomal recessive disorder characterized by degeneration of spin...
The spinal muscular atrophies are a group of mostly inherited disorders selectively affecting the lo...
Spinal muscular atrophy (SMA) is one of the most common autosomal recessive disorders characterized ...
Childhood proximal spinal muscular atrophy (SMA) is an autosomal recessive disorder which presents a...
Deletions of the spinal muscular atrophy (SMA)-determining gene, SMN1, NAIP, and a third multicopy g...
Spinal muscular atrophies (SMAs) are a heterogeneous group of neuromuscular diseases characterized b...
Spinal muscular atrophy (SMA) is caused by functional loss of the survival of motor neuron 1 (SMN...
Spinal muscular atrophy (SMA) is one of the most common autosomal recessive diseases, affecting apro...
SummaryProximal spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disorder cause...
[[abstract]]Mutations of the telomeric survival motor neuron gene (SMN1) are related to spinal muscu...
Background: Proximal spinal muscular atrophy (SMA) is a genetically heterogeneous disease with pares...
Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disorder which affects α-motor...
AbstractObjectiveAutosomal recessive spinal muscular atrophy (SMA) is, after cystic fibrosis, the se...
The spinal muscular atrophies are a group of disorders characterized by flaccid limb weakness. It is...
Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disease characterized by regen...
Spinal muscular atrophy (SMA) is autosomal recessive disorder characterized by degeneration of spin...
The spinal muscular atrophies are a group of mostly inherited disorders selectively affecting the lo...
Spinal muscular atrophy (SMA) is one of the most common autosomal recessive disorders characterized ...
Childhood proximal spinal muscular atrophy (SMA) is an autosomal recessive disorder which presents a...
Deletions of the spinal muscular atrophy (SMA)-determining gene, SMN1, NAIP, and a third multicopy g...
Spinal muscular atrophies (SMAs) are a heterogeneous group of neuromuscular diseases characterized b...
Spinal muscular atrophy (SMA) is caused by functional loss of the survival of motor neuron 1 (SMN...
Spinal muscular atrophy (SMA) is one of the most common autosomal recessive diseases, affecting apro...
SummaryProximal spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disorder cause...
[[abstract]]Mutations of the telomeric survival motor neuron gene (SMN1) are related to spinal muscu...
Background: Proximal spinal muscular atrophy (SMA) is a genetically heterogeneous disease with pares...
Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disorder which affects α-motor...
AbstractObjectiveAutosomal recessive spinal muscular atrophy (SMA) is, after cystic fibrosis, the se...
The spinal muscular atrophies are a group of disorders characterized by flaccid limb weakness. It is...
Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disease characterized by regen...
Spinal muscular atrophy (SMA) is autosomal recessive disorder characterized by degeneration of spin...
The spinal muscular atrophies are a group of mostly inherited disorders selectively affecting the lo...