A GTG to ATG novel point mutation at codon 804 in exon 14 of the RET proto-oncogene in two families affected by familial medullary thyroid carcinoma-Reference-Cited by-同舟云学术

A GTG to ATG novel point mutation at codon 804 in exon 14 of the RET proto-oncogene in two families affected by familial medullary thyroid carcinoma

Published:1998 Issue:S1 Volume:11 Page:S167-S171
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Fattoruso Olimpia,Quadro Loredana,Libroia Alfonso,Verga Uberta,Lupoli Giovanni,Cascone Edvige,Colantuoni Vittorio

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference20 articles.

1. RET mutations in exons 13 and 14 of FMTC patients;Bolino;Oncogene,1995

2. Additional RFLPs at D10S94 and the development of PCR. Based variant detection systems: implications for disease genotype prediction in MEN 2A, MEN 2B and MTC families;Brooks-Wilson;Genomics,1992

3. DNA polymorphisms and conditions for SSCP analysis of the 20 exons of the RET proto-oncogene;Ceccherini;Oncogene,1994

4. Mutations in the RET proto-oncogene are associated with MEN2A and FMTC;Donis-Keller;Hum Mol Genet,1993

5. A novel point mutation in the tyrosine kinase domain of the RET proto-oncogene in sporadic medullary thyroid carcinoma and in a family with FMTC;Eng;Oncogene,1995

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