The familial medullary thyroid carcinoma-associated RET E768D mutation in a multiple endocrine neoplasia type 2A case-Reference-Cited by-同舟云学术

The familial medullary thyroid carcinoma-associated RET E768D mutation in a multiple endocrine neoplasia type 2A case

Published:2005-05 Issue:5 Volume:137 Page:574-576
ISSN:0039-6060
Container-title:Surgery
language:en
Short-container-title:Surgery

Author:

Aiello Antonella,Cioni Katia,Gobbo Morena,Collini Paola,Gullo Maria,Torre Gabriella Della,Passerini Emanuele,Ferrando Barbara,Pilotti Silvana,Pierotti Marco A.,Pasini Barbara

Publisher

Elsevier BV

Subject

Surgery

Reference6 articles.

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2. Guidelines for diagnosis and therapy of MEN type 1 and type 2;Brandi;J Clin Endocrinol Metab,2001

3. V804M RET mutation in MEN 2A: first report;Scacheri;Intern Med,2004

4. Pheochromocytoma and medullary thyroid carcinoma: a new genotype-phenotype correlation of the RET proto-oncogene 891 germline mutation;Jimenez;J Clin Endocrinol Metab,2004

5. A novel germ-line point mutation in RET exon 8 (Gly(533)Cys) in a large kindred with familial medullary thyroid carcinoma;Da Silva;J Clin Endocrinol Metab,2003

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