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Developmental and degenerative cardiac defects in the Taiwanese mouse model of severe spinal muscular atrophy
Spinal muscular atrophy (SMA), an autosomal recessive disease caused by a decrease in levels of the survival motor neuron (SMN) protein, is the most common genetic cause of infant mortality. Although neuromuscular pathology is the most severe feature of SMA, other organs and tissues, including the h...
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| Pubblicato in: | J Anat |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
John Wiley and Sons Inc.
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5978979/ https://ncbi.nlm.nih.gov/pubmed/29473159 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/joa.12793 |
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