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Fabry disease: Evidence for a regional founder effect of the GLA gene mutation 30delG in Brazilian patients
The Fabry disease is caused by mutations in the gene (GLA) that encodes the enzyme α-galactosidase A (α-Gal A). More than 500 pathologic variants of GLA have already been described, most of them are family-specific. In southern Brazil, a frequent single-base deletion (GLA 30delG) was identified amon...
| Autores principales: | , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2014
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5121364/ https://www.ncbi.nlm.nih.gov/pubmed/27896116 http://dx.doi.org/10.1016/j.ymgmr.2014.09.002 |