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Novel compound heterozygote mutations in the ATP7B gene in an Iranian family with Wilson disease: a case report. [electronic resource]

By:

Daneshjoo, Omid

Contributor(s):

Garshasbi, Masoud

Producer: 20180917Description: 68 p. digitalISSN:

1752-1947

Subject(s):

Online resources:

Available from publisher's website

In: Journal of medical case reports vol. 12

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Publication Type: Case Reports; Journal Article

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