Mutation of RET codon 768 is associated with the FMTC phenotype
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1997.tb02424.x/fullpdf
Reference24 articles.
1. Recommendations for standardized human pedigree nomenclature;Bennett;Am J Hum Genet,1995
2. RET mutations in exons 13 and 14 of FMTC patients;Bolino;Oncogene,1995
3. Single missense mutation in the tyrosine kinase catalytic domain of the RET proto-oncogene is associated with multiple endocrine neoplasia type 2B;Carlson;Proc Natl Acad Sci USA,1994
4. Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC;Donis-Keller;Hum Mol Genet,1993
5. Point mutations within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours;Eng;Hum Mol Genet,1994
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