Medicine
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12 june 2020 18:41:32 |
| Genotype-phenotype variable correlation in Wilson disease: clinical history of two sisters with the similar genotype (BMC Medical Genetics) |
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Tweet Wilson disease (WD) is an Autosomal-Recessive disorder due to mutations of ATP7B gene on chromosome 13q14.3. Inadequate protein function leads to low ceruloplasmin blood levels and copper accumulation in liver, b... |
| 288 viewsCategory: Genetics, Medicine |
 Osteoprotegerin gene polymorphisms and otosclerosis: an additional genetic association study, multilocus interaction and meta-analysis (BMC Medical Genetics)Genetic variants of VDR and CYP2R1 affect BMI independently of serum vitamin D concentrations (BMC Medical Genetics) 
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