{
    "PMID": "10664228",
    "TI": "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.",
    "JT": "European journal of pediatrics",
    "BTI": "",
    "DP": "2000-03",
    "AU": "Sakai T, Nirasawa Y, Itoh Y, Wakizaka A"
}
