Associated Papers
Novel mutations of endothelin-B receptor gene in Pakistani patients with Waardenburg syndrome.
Jabeen R et al.
Molecular Biology Reports, 2012
Double heterozygosity for a RET substitution interfering with splicing and an EDNRB missense mutation in Hirschsprung disease.
Auricchio A et al.
American Journal of Human Genetics, 1999
Endothelin-B receptor mutations in patients with isolated Hirschsprung disease from a non-inbred population.
Auricchio A et al.
Human Molecular Genetics, 1996
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