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 - Sakai, T.; Nirasawa, Y.; Itoh, Y.; Wakizaka, A. (European journal of pediatrics, 2000)
Keywords: Asian Continental Ancestry Group - genetics; Biological and medical sciences; DNA Mutational Analysis; Drosophila Proteins; Endothelin-3 - genetics; Female; Gastroenterology. Liver. Pancreas. Abdomen; Genes; Genetic Predisposition to Disease; Glial Cell Line-Derived Neurotrophic Factor; Glial Cell Line-Derived Neurotrophic Factor Receptors; Hirschsprung Disease - genetics; Humans; Japan; Kinases; Male; Malformations; Medical sciences; Mutation; Nerve Growth Factors - genetics; Nerve Tissue Proteins - genetics; Neurturin; Pathogenesis; Polymerase chain reaction; Proto-Oncogene Proteins - genetics; Proto-Oncogene Proteins c-ret; Receptor Protein-Tyrosine Kinases - genetics; Receptor, Endothelin B; Receptors, Endothelin - genetics; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus; Japan; Human; Endothelin; Neuronal intestinal malformation; Endothelin 3; Congenital disease; Genetic determinism; Colonic disease; Hirschsprung disease; Glial cell line derived neurotrophic factor; Digestive diseases; Intestinal disease; Mutation; Protooncogene; Biological receptor