SNP information rs1801248
Normal allele: CC
Polymorphisms associated with Wilson's disease. Wilson's disease is an inherited disorder in which excess copper is stored in the body.
Polymorphism rs1801248 is related to topics like this:
Wilson's disease is an autosomal recessive condition, necessitating that both parents carry at...
Research and publications:
8533760 Molecular pathology and haplotype analysis of Wilson disease in Mediterranean populations.
16088907 Twenty-four novel mutations in Wilson disease patients of predominantly European ancestry.
While the body requires only minuscule quantities of the trace mineral molybdenum, it serves as a...
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