Investigation of germline GFRα-1 mutations in Hirschsprung disease

Inactivating mutations of the RET proto-oncogene and of one of its soluble ligand molecules, glial cell line derived neurotrophic factor (GDNF), have been found in a subset of patients with Hirschsprung disease (HSCR). However, the majority of HSCR mutations remain unidentified. As normal RET functi...

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Detalhes bibliográficos
Main Authors: Myers, S., Salomon, R., Goessling, A., Pelet, A., Eng, C., von Deimling, A., Lyonnet, S., Mulligan, L.
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 1999
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1734319/
https://ncbi.nlm.nih.gov/pubmed/10204848
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