Multiple endocrine neoplasia syndromes, children, Hirschsprung’s disease and RET
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Surgery,Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s00383-008-2137-5.pdf
Reference109 articles.
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2. Akhand AA, Ikeyama T, Akazawa S, Kato M, Hossain K, Takeda K, Suzuki H, Takahashi M, Nakashima I (2002) Evidence of both extra- and intracellular cysteine targets of protein modification for activation of RET kinase. Biochem Biophys Res Commun 292(4):826–831
3. Antinolo G, Marcos I, Fernandez RM, Romero M, Borrego S (2002) A novel germline point mutation, c.2304 G–>T, in codon 768 of the RET proto-oncogene in a patient with medullary thyroid carcinoma. Am J Med Genet 110(1):85–87
4. Arighi E, Popsueva A, Degl’Innocenti D, Borrello MG, Carniti C, Perala NM, Pierotti MA, Sariola H (2004) Biological effects of the dual phenotypic Janus mutation of ret cosegregating with both multiple endocrine neoplasia type 2 and Hirschsprung’s disease. Mol Endocrinol 18(4):1004–1017
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