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JMG.33.6.521
JMG.33.6.521
http://dx.doi.org/10.1136/JMG.33.6.521
High frequency of two mutations in codon 778 in exon 8 of the ATP7B gene in Taiwanese families with Wilson disease.
P356
Q33677490-2009D204-9413-419D-A697-94F67927A9D4
P356
JMG.33.6.521
http://dx.doi.org/10.1136/JMG.33.6.521