Deletion of SMN and NAIP genes in Korean patients with spinal muscular atrophy.

Childhood-onset proximal spinal muscular atrophies (SMAs) are an autosomal recessive, clinically heterogeneous group of neuronopathies characterized by selective degeneration of anterior horn cells. The causative genes to be reported are survival motor neuron (SMN) and neuronal apoptosis inhibitory...

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Autors principals: Shin, S., Park, S. S., Hwang, Y. S., Lee, K. W., Chung, S. G., Lee, Y. J., Park, M. H.
Format: Artigo
Idioma:Inglês
Publicat: Korean Academy of Medical Sciences 2000
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Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3054589/
https://ncbi.nlm.nih.gov/pubmed/10719817
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