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The mutation of the Wilsons disease protein ATP7B has been widely used to study the direct link between hepatic high copper and development of liver pathology
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This guide explains W54.0XXA, body-site specificity, encounter types, and how to avoid costly denials
Optic Nerve Atrophy: Use with caution in patients with Leber's diseasea type of hereditary optic nerve atrophyas it may worsen the condition
