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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Detalles Bibliográficos
Autores principales: Shin, S., Park, S. S., Hwang, Y. S., Lee, K. W., Chung, S. G., Lee, Y. J., Park, M. H.
Formato: Texto
Lenguaje:English
Publicado: Korean Academy of Medical Sciences 2000
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054589/
https://www.ncbi.nlm.nih.gov/pubmed/10719817

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054589/
https://www.ncbi.nlm.nih.gov/pubmed/10719817

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