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Fatty Acyl-CoA Reductase 1 Deficiency
Investigators from Erlangen, Germany; Calgary, CA; and Kafranbel, Syria, identified mutations in the gene, fatty acyl-CoA reductase 1 (FAR1) deficiency, adding to three other genes involved in plasmalogen biosynthesis, in two families affected by severe intellectual disability, early-onset epilepsy,...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Pediatric Neurology Briefs Publishers
2015
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4747304/ https://www.ncbi.nlm.nih.gov/pubmed/26933529 http://dx.doi.org/10.15844/pedneurbriefs-29-1-5 |