Mutations of the RET-GDNF Signaling Pathway in Ondine's Curse
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics
Reference17 articles.
1. Germline mutation in glial cell line–derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient;Angrist;Nat Genet,1996
2. Heterozygous endothelin receptor B (EDNRB) mutations in Hirschsprung disease;Amiel;Hum Mol Genet,1996
3. Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung disease;Attié;Hum Mol Genet,1995
4. Mutation of the endothelin-receptor B gene in the Waardenburg-Hirschsprung disease;Attié;Hum Mol Genet,1995
5. The neurocristopathies: a unifying concept of disease arising in neural crest maldevelopment;Bolande;Hum Pathol,1973
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