Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas.

Phaeochromocytomas may occur sporadically, or as part of the inherited cancer syndromes multiple endocrine neoplasia (MEN) type 2, von Hippel-Lindau disease (VHL), and, rarely, in type 1 neurofibromatosis. In MEN 2, germline missense mutations have been found in one of eight codons within exons 10,...

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Autors principals: Eng, C, Crossey, P A, Mulligan, L M, Healey, C S, Houghton, C, Prowse, A, Chew, S L, Dahia, P L, O'Riordan, J L, Toledo, S P
Format: Artigo
Idioma:Inglês
Publicat: 1995
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Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051771/
https://ncbi.nlm.nih.gov/pubmed/8825918
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