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,...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: 1995
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051771/
https://ncbi.nlm.nih.gov/pubmed/8825918
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados