De novo deletions in spinal muscular atrophy: implications for genetic counselling.
AUTOR(ES)
Raclin, V
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1050854Documentos Relacionados
- Chronic proximal spinal muscular atrophy of childhood and adolescence: problems of classification and genetic counselling.
- Spinal Muscular Atrophy: Infantile and Juvenile Type
- Gene deletions in spinal muscular atrophy.
- Spinal motor neurones in murine muscular dystrophy and spinal muscular atrophy: A quantitative histological study
- Motor nerve conduction velocity in peroneal muscular atrophy: evidence for genetic heterogeneity