Various Penetrance of Familial Medullary Thyroid Carcinoma in Patients With RET Protooncogene Codon 790/791 Germline Mutations

OBJECTIVE: To describe a genotype–phenotype correlation in MEN2 families with RET germline mutations of codons 790/791 and discuss options for the therapeutic management of gene carriers. SUMMARY BACKGROUND DATA: Heredity of MEN2 syndromes is caused by a heterozygous germline mutation in the RET pro...

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Main Authors: Fitze, Guido, Schierz, Mandy, Bredow, Jan, Saeger, Hans D., Roesner, Dietmar, Schackert, Hans K.
Formato: Artigo
Idioma:Inglês
Publicado em: 2002
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1422614/
https://ncbi.nlm.nih.gov/pubmed/12409662
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