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Article

Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient

1 Nov 1996

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 8896568
DOI: 10.1038/ng1196-341

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Related research

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Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patientPMID 8896568Read ↗

New mutations associated with Hirschsprung disease.Semantic proximity Read ↗

[New mutations associated with Hirschsprung disease].Semantic proximity Read ↗

Double Heterozygosity for a RET Substitution Interfering with Splicing and an EDNRB Missense Mutation in Hirschsprung DiseaseSemantic proximity Read ↗

RET somatic mutations are underrecognized in Hirschsprung disease.Semantic proximity Read ↗

Non-syndromic Hirschsprung's disease as a result of a RET gene variant.Semantic proximity Read ↗

Highly recurrent RET mutations and novel mutations in genes of the receptor tyrosine kinase and endothelin receptor B pathways in Chinese patients with sporadic Hirschsprung disease.Semantic proximity Read ↗

Genetics of Hirschsprung diseaseSemantic proximity Read ↗

Advances in molecular genetics of Hirschsprung's disease.Semantic proximity Read ↗

Phenotypic variation in a family with mutations in two Hirschsprung-related genes (RET and endothelin receptor B).Semantic proximity Read ↗

Incidence of RET mutations in patients with Hirschsprung's diseaseSemantic proximity Read ↗

Molecular heterogeneity of RET loss of function in Hirschsprung's disease.Semantic proximity Read ↗

Identification of a novel variant of the RET proto-oncogene in a novel family with Hirschsprung's disease.Semantic proximity Read ↗

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