Add to ORKGWilson disease (WD) is an autosomal recessive disorder of copper metabolism that results in accumulation of copper in the liver, brain, cornea, kidney, and other tissues (1). WD i
Wilson disease (WD) is an autosomal recessive disorder of copper transport. WD patients are presenti...
Wilson's disease is a rare autosomal recessive disorder characterized by accumulation of copper in t...
Wilson’s disease (WD) is a rare autosomal recessive disorder of hepatocellular copper deposition. Th...
Wilsons disease (WD) (hepatolenticular degeneration, Westphal-Strumpell disease) is a genetic disord...
Wilson’s disease is an autosomal recessive disorder of copper metabolism characterized by excessive ...
Wilson disease is an autosomal recessive copper storage disease. It is characterized by an inability...
Wilson disease is an autosomal recessive copper storage disease. It is characterized by an inability...
Wilson's disease (WD) is a copper metabolism disorder that is inherited in an autosomal recessive ma...
Wilson’s disease (WD), also known as hepatolenticular degeneration, is an autosomal recessive inheri...
Wilson’s disease is an autosomal recessive disorder of copper metabolism that causes accumulation of...
WOS: 000360663100023Wilson disease (WD) is an autosomal recessive disorder of copper transport cause...
Wilson disease is an inherited autosomal recessive disorder of hepatic copper metabolism leading to ...
Wilson`s disease (hepatolenticular degeneration) is an autosomal recessive dis or der of copper tran...
Wilson’s disease is a rare autosomal recessive disorder characterized by accumulation of copper in t...
Wilson disease is an inherited, autosomal recessive, copper accumulation and toxicity disorder that ...
Wilson disease (WD) is an autosomal recessive disorder of copper transport. WD patients are presenti...
Wilson's disease is a rare autosomal recessive disorder characterized by accumulation of copper in t...
Wilson’s disease (WD) is a rare autosomal recessive disorder of hepatocellular copper deposition. Th...
Wilsons disease (WD) (hepatolenticular degeneration, Westphal-Strumpell disease) is a genetic disord...
Wilson’s disease is an autosomal recessive disorder of copper metabolism characterized by excessive ...
Wilson disease is an autosomal recessive copper storage disease. It is characterized by an inability...
Wilson disease is an autosomal recessive copper storage disease. It is characterized by an inability...
Wilson's disease (WD) is a copper metabolism disorder that is inherited in an autosomal recessive ma...
Wilson’s disease (WD), also known as hepatolenticular degeneration, is an autosomal recessive inheri...
Wilson’s disease is an autosomal recessive disorder of copper metabolism that causes accumulation of...
WOS: 000360663100023Wilson disease (WD) is an autosomal recessive disorder of copper transport cause...
Wilson disease is an inherited autosomal recessive disorder of hepatic copper metabolism leading to ...
Wilson`s disease (hepatolenticular degeneration) is an autosomal recessive dis or der of copper tran...
Wilson’s disease is a rare autosomal recessive disorder characterized by accumulation of copper in t...
Wilson disease is an inherited, autosomal recessive, copper accumulation and toxicity disorder that ...
Wilson disease (WD) is an autosomal recessive disorder of copper transport. WD patients are presenti...
Wilson's disease is a rare autosomal recessive disorder characterized by accumulation of copper in t...
Wilson’s disease (WD) is a rare autosomal recessive disorder of hepatocellular copper deposition. Th...