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Wilson’s disease in Lebanon and regional countries: Homozygosity and hepatic phenotype predominance
AIM: To determine the phenotypes and predominant disease-causing mutations in Lebanese patients with Wilson’s disease, as compared to regional non-European data. METHODS: The clinical profile of 36 patients diagnosed in Lebanon was studied and their mutations were determined by molecular testing. Al...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Baishideng Publishing Group Inc
2017
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5643292/ https://www.ncbi.nlm.nih.gov/pubmed/29085216 http://dx.doi.org/10.3748/wjg.v23.i36.6715 |