Germ-line mutation analysis in patients with multiple endocrine neoplasia type 1 and related disorders.

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant syndrome predisposing to tumors of the parathyroid, endocrine pancreas, anterior pituitary, adrenal glands, and diffuse neuroendocrine tissues. The MEN1 gene has been assigned, by linkage analysis and loss of heterozygosity, to chro...

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Autori principali: Giraud, S, Zhang, C X, Serova-Sinilnikova, O, Wautot, V, Salandre, J, Buisson, N, Waterlot, C, Bauters, C, Porchet, N, Aubert, J P, Emy, P, Cadiot, G, Delemer, B, Chabre, O, Niccoli, P, Leprat, F, Duron, F, Emperauger, B, Cougard, P, Goudet, P, Sarfati, E, Riou, J P, Guichard, S, Rodier, M, Meyrier, A, Caron, P, Vantyghem, M C, Assayag, M, Peix, J L, Pugeat, M, Rohmer, V, Vallotton, M, Lenoir, G, Gaudray, P, Proye, C, Conte-Devolx, B, Chanson, P, Shugart, Y Y, Goldgar, D, Murat, A, Calender, A
Natura: Artigo
Lingua:Inglês
Pubblicazione: 1998
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Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377295/
https://ncbi.nlm.nih.gov/pubmed/9683585
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