[Spinal muscular atrophy: frequent cause of congenital hypotonia in Morocco]. [electronic resource]
Producer: 20120511Description: 1261-4 p. digitalISSN:- 1769-664X
- Child, Preschool
- DNA
- Electromyography
- Exons
- Gene Deletion
- Genetic Counseling
- Genetic Testing
- Genome, Human
- Humans
- Infant
- Infant, Newborn
- Morocco -- epidemiology
- Muscle Hypotonia -- congenital
- Prevalence
- Spinal Muscular Atrophies of Childhood -- diagnosis
- Survival of Motor Neuron 1 Protein -- genetics
- Survival of Motor Neuron 2 Protein -- genetics
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Publication Type: English Abstract; Journal Article
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