TY  - GEN
AU  - Sbiti,A
AU  - Ratbi,I
AU  - Kriouile,Y
AU  - Sefiani,A
TI  - [Spinal muscular atrophy: frequent cause of congenital hypotonia in Morocco]
SN  - 1769-664X
PY  - 2012///0511
KW  - Child, Preschool
KW  - DNA
KW  - Electromyography
KW  - Exons
KW  - Gene Deletion
KW  - Genetic Counseling
KW  - Genetic Testing
KW  - Genome, Human
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Morocco
KW  - epidemiology
KW  - Muscle Hypotonia
KW  - congenital
KW  - Prevalence
KW  - Spinal Muscular Atrophies of Childhood
KW  - diagnosis
KW  - Survival of Motor Neuron 1 Protein
KW  - genetics
KW  - Survival of Motor Neuron 2 Protein
N1  - Publication Type: English Abstract; Journal Article
UR  - https://doi.org/10.1016/j.arcped.2011.09.025
ER  -