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A novel PCCB mutation in a Thai patient with propionic acidemia identified by exome sequencing
Propionic acidemia (PA) is an inborn error of metabolism, caused by mutations in either the PCCA or PCCB gene, leading to mitochondrial accumulation of propionyl-CoA and its by-products. Here we report a 6-year-old Thai boy with PA who was born to consanguineous parents. Exome sequencing identified...
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| Publicado no: | Hum Genome Var |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4785532/ https://ncbi.nlm.nih.gov/pubmed/27081542 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/hgv.2015.33 |
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