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Hyperleptinemia in children with autosomal recessive spinal muscular atrophy type I-III
BACKGROUND: Autosomal-recessive proximal spinal muscular atrophies (SMA) are disorders characterized by a ubiquitous deficiency of the survival of motor neuron protein that leads to a multisystemic disorder, which mostly affects alpha motor neurons. Disease progression is clinically associated with...
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| Pubblicato in: | PLoS One |
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| Autori principali: | , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Public Library of Science
2017
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5344335/ https://ncbi.nlm.nih.gov/pubmed/28278160 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0173144 |
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