Identification of MEN1 gene mutations in families with MEN 1 and related disorders

Following identification of the MEN1 gene, we analysed patients from 12 MEN 1 families, 8 sporadic cases of MEN 1, and 13 patients with MEN 1-like symptoms (e.g. cases of familial isolated hyperparathyroidism (FIHPT), familial acromegaly, or atypical MEN 1 cases) for the presence of germline MEN1 mu...

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Detalles Bibliográficos
Autores principales: Bergman, L, Teh, B, Cardinal, J, Palmer, J, Walters, M, Shepherd, J, Cameron, D, Hayward, N
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2000
Materias:
Regular Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363562/
https://www.ncbi.nlm.nih.gov/pubmed/10993647
http://dx.doi.org/10.1054/bjoc.2000.1380

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363562/
https://www.ncbi.nlm.nih.gov/pubmed/10993647
http://dx.doi.org/10.1054/bjoc.2000.1380

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