Wilson Disease in a Turkish Population: Molecular Insights into an Old Disease with Reported and Novel Variants
Objective: Wilson’s disease (WD) is a rare autosomal recessive genetic liver disorder with hepatic, neurological, or psychiatric manifestations between 1st to 5th decades. WD is caused by homozygous or compound heterozygous pathogenic variants in the ATP7B gene. In this study, we aimed to contribute...
Sábháilte in:
| Príomhchruthaitheoirí: | , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe / Cruthaithe: |
Galenos Publishing House
2024-04-01
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| Sraith: | Gazi Medical Journal |
| Ábhair: | |
| Rochtain ar líne: | https://gazimedj.com/articles/wilson-disease-in-a-turkish-population-molecular-insights-into-an-old-disease-with-reported-and-novel-variants/doi/gmj.2023.3795 |
| Clibeanna: |
Níl clibeanna ann, Bí ar an gcéad duine le clib a chur leis an taifead seo!
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