DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
LinksClose Window
References
Kimura S, Ikezawa M, Ozasa S. et al.
Novel mutation in splicing donor of dystrophin gene first exon in a patient with dilated cardiomyopathy but no clinical signs of skeletal myopathy.
J Child Neurol 2007;
22 (07) 901-906
Access:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.