Associated Papers
Identification of a novel mutation in a Chinese family with Nance-Horan syndrome by whole exome sequencing.
Hong N et al.
Journal of Zhejiang University. Science. B, 2014
Mutational analysis of Peroxiredoxin IV: exclusion of a positional candidate for multinodular goitre.
Giardina E et al.
Bmc Medical Genetics, 2002
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