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Fig. 4 | BMC Gastroenterology

Fig. 4

From: Mutation analysis of the ATP7B gene and genotype–phenotype correlation in Chinese patients with Wilson disease

Fig. 4

A Correlation of 3884C>T (Ala1295Val) and clinical manifestations; B correlation of 2333G>T (Arg778 Leu) and serum ceruloplasmin level; C correlation of 2975C>T (Pro992Leu) and the onset age; D correlation of 3809 A>G (Asn1270Ser) and the onset age. Homo homozygotes for the mutation, Hetero heterozygotes for the mutation, H hepatic manifestation, N neurological manifestation, M mixed manifestation

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