[Spinal muscular atrophy: frequent cause of congenital hypotonia in Morocco]. [electronic resource]
- Archives de pediatrie : organe officiel de la Societe francaise de pediatrie Dec 2011
- 1261-4 p. digital
Publication Type: English Abstract; Journal Article
1769-664X
10.1016/j.arcped.2011.09.025 doi
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