Associated Papers
Tyrosinemia type II: Mutation update, 11 novel mutations and description of 5 independent subjects with a novel founder mutation.
Peña-Quintana L et al.
Clinical Genetics, 2017
A large TAT deletion in a tyrosinaemia type II patient.
Legarda M et al.
Molecular Genetics and Metabolism, 2011
Tyrosinemia type II (Richner-Hanhart syndrome): a new mutation in the TAT gene.
Culic V et al.
European Journal of Medical Genetics, 0
Select a paper to view details