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Article

A missense mutation of the endothelin-B receptor gene in multigenic hirschsprung's disease

1 Dec 1994

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 8001158
DOI: 10.1016/0092-8674(94)90016-7

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A missense mutation of the endothelin-B receptor gene in multigenic hirschsprung's diseasePMID 8001158Read ↗

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Functional characterization of three mutations of the endothelin B receptor gene in patients with Hirschsprung's disease: evidence for selective loss of Gi coupling.Semantic proximity Read ↗

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