DOI: 10.1055/s-00000041

Neuropediatrics

References

Hutchinson DO, Charlton A, Graham L, Laing N, Ilkovski B, North KN.
Autosomal dominant nemaline myopathy with intranuclear rods due to a mutation of the skeletal muscle ACTA1 gene: clinical and pathological variability within a kindred. 
Neuromuscul Disord 2006; 16: 113-121  

Download Bibliographical Data

Search in:
Access:
Access: