Mutations of the RET-GDNF Signaling Pathway in Ondine's Curse
- 1 March 1998
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 62 (3) , 715-717
- https://doi.org/10.1086/301759
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- RET proto-oncogene is important for the development of respiratory CO2 sensitivityJournal of the Autonomic Nervous System, 1997
- Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patientNature Genetics, 1996
- Endothelin–3 frameshift mutation in congenital central hypoventilation syndromeNature Genetics, 1996
- Congenital central hypoventilation syndrome: Mutation analysis of the receptor tyrosine kinase RETAmerican Journal of Medical Genetics, 1996
- GDNF signalling through the Ret receptor tyrosine kinaseNature, 1996
- Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome)Nature Genetics, 1996
- Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprung diseaseHuman Molecular Genetics, 1996
- Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung diseaseHuman Molecular Genetics, 1995
- CONGENITAL FAILURE OF AUTOMATIC CONTROL OF VENTILATION, GASTROINTESTINAL MOTILITY AND HEART RATEMedicine, 1978
- The neurocristopathiesA unifying concept of disease arising in neural crest maldevelopmentHuman Pathology, 1974