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JCI115979
JCI115979
http://dx.doi.org/10.1172/JCI115979
Type 1 hereditary tyrosinemia. Evidence for molecular heterogeneity and identification of a causal mutation in a French Canadian patient
P356
Q24564762-7D0265A8-E04C-447A-82FD-4110F83523CF
P356
JCI115979
http://dx.doi.org/10.1172/JCI115979