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Japanese patients with sporadic Hirschsprung: mutation analysis of the receptor tyrosine kinase proto-oncogene, endothelin-B receptor, endothelin-3, glial cell line-derived neurotrophic factor and neurturin genes: a comparison with similar studies

Mendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseSporadic HirschsprungEndothelin-b ReceptorPathologyDegenerative DiseaseDisease Gene IdentificationMedicineJapanese Patients