[From gene to disease; Wilson disease: copper storage due to mutations in ATP7B]
- PMID: 12892020
[From gene to disease; Wilson disease: copper storage due to mutations in ATP7B]
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[From gene to disease; Wilson disease: copper storage due to mutations in ATP7B].Ned Tijdschr Geneeskd. 2003 Mar 29;147(13):603-5. Ned Tijdschr Geneeskd. 2003. PMID: 12701394 Review. Dutch.
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[From gene to disease; Wilson disease: copper storage due to mutations in ATP7B].Ned Tijdschr Geneeskd. 2003 Mar 29;147(13):603-5. Ned Tijdschr Geneeskd. 2003. PMID: 12701394 Review. Dutch.
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