Disturbed copper transport in humans. Part 2: mutations of the ATP7B gene lead to Wilson disease (WD). (Q43950092)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Disturbed copper transport in humans. Part 2: mutations of the ATP7B gene lead to Wilson disease (WD). |
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Disturbed copper transport in humans. Part 2: mutations of the ATP7B gene lead to Wilson disease (WD). (English)
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Seidel J
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Caca K
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Schwab SG
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Berr F
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Wildenauer DB
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Mentzel HJ
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Horn N
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Kauf E
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1 January 2001
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47 Online Pub
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OL149-57
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Identifiers
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