Case/control family study of autonomic nervous system dysfunction in idiopathic congenital central hypoventilation syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference48 articles.
1. Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprung disease
2. Mutations of the RET-GDNF Signaling Pathway in Ondine's Curse
3. Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease
4. Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient
5. Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung disease
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5. Paired-like homeobox gene (PHOX2B) nonpolyalanine repeat expansion mutations (NPARMs): genotype–phenotype correlation in congenital central hypoventilation syndrome (CCHS);Genetics in Medicine;2021-09
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