Oncological implications of RET gene mutations in Hirschsprung's disease

Background—Germline mutations of the RET proto-oncogene identical to those found in the tumour predisposition syndrome multiple endocrine neoplasia type 2A (MEN2A), were detected in 2.5-5% of sporadic and familial cases of Hirschsprung's disease. Some patients with Hirschsprung's disease m...

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Huvudupphovsmän: Sijmons, R, Hofstra, R, Wijburg, F, Links, T, Zwierstra, R, Vermey, A, Aronson, D, Tan-Sindhunata, G, Brouwers-Smalbraa..., G, Maas, S, Buys, C
Materialtyp: Artigo
Språk:Inglês
Publicerad: 1998
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Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC1727297/
https://ncbi.nlm.nih.gov/pubmed/9824583
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