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Newborn genetic screening for spinal muscular atrophy in the UK: The views of the general population
BACKGROUND: Spinal muscular atrophy (SMA) is an inherited neuromuscular disorder and a leading genetic cause of infant death worldwide. However, there is no routine screening program for SMA in the UK. Lack of treatments and the inability of screening tests to accurately predict disease severity are...
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| Publicado no: | Mol Genet Genomic Med |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5823674/ https://ncbi.nlm.nih.gov/pubmed/29169204 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.353 |
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