Associated Papers
Whole Exome Sequencing Identifies a Novel Pathogenic RET Variant in Hirschsprung Disease.
Wu W et al.
Frontiers in Genetics, 2018
Highly recurrent RET mutations and novel mutations in genes of the receptor tyrosine kinase and endothelin receptor B pathways in Chinese patients with sporadic Hirschsprung disease.
Garcia-Barceló M et al.
Clinical Chemistry, 2004
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