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Hypoxia at the heart of sudden infant death syndrome?
Sudden infant death syndrome (SIDS) remains a significant clinical problem without an accepted pathological mechanism, but with multiple conflicting models. Mutation in a growing number of genes has been found post mortem in SIDS cases, notably genes encoding ion channels. This can only account for...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
2013
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3977030/ https://www.ncbi.nlm.nih.gov/pubmed/23863852 http://dx.doi.org/10.1038/pr.2013.122 |