Congenital central hypoventilation syndrome associated with Hirschsprung's disease: Mutation analysis of the RET and endothelin-signaling pathways

European Journal of Pediatric Surgery

Volumn 11, Issue 5, 2001, Pages 335-337

  Sakai, T ^a   Wakizaka, A ^a   Nirasawa, Y ^a  

^a KYORIN UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

CCHS; EDNRB; HSCR; Neurocristopathy; RET proto oncogene

Indexed keywords

ENDOTHELIN B RECEPTOR; PROTEIN TYROSINE KINASE;

ARTICLE; CASE REPORT; CELL DIFFERENTIATION; CELL MIGRATION; CELL PROLIFERATION; CHILD; DISEASE ASSOCIATION; EXON; FEMALE; GENE MUTATION; GENETIC CODE; GENETIC POLYMORPHISM; HIRSCHSPRUNG DISEASE; HUMAN; HYPOVENTILATION; INCIDENCE; MALE; MODULATION; NEURAL CREST CELL; PATHOGENESIS; SIGNAL TRANSDUCTION;

CHILD; DNA MUTATIONAL ANALYSIS; DROSOPHILA PROTEINS; EXONS; FEMALE; HIRSCHSPRUNG DISEASE; HUMANS; MALE; POLYMERASE CHAIN REACTION; PROTO-ONCOGENE PROTEINS; PROTO-ONCOGENE PROTEINS C-RET; RECEPTOR PROTEIN-TYROSINE KINASES; RECEPTOR, ENDOTHELIN B; RECEPTORS, ENDOTHELIN; SLEEP APNEA SYNDROMES;

EID: 0035154068     PISSN: 09397248     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2001-18552     Document Type: Article

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