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A survey of transcripts generated by spinal muscular atrophy genes

Human Survival Motor Neuron (SMN) genes code for SMN, an essential multifunctional protein. Complete loss of SMN is embryonic lethal, while low levels of SMN lead to spinal muscular atrophy (SMA), a major genetic disease of children and infants. Reduced levels of SMN are associated with the abnormal...

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Detalles Bibliográficos
Publicado en:Biochim Biophys Acta Gene Regul Mech
Main Authors: Singh, Natalia N., Ottesen, Eric W., Singh, Ravindra N.
Formato: Artigo
Idioma:Inglês
Publicado: 2020
Assuntos:
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC7302838/
https://ncbi.nlm.nih.gov/pubmed/32387331
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbagrm.2020.194562
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