A novel germline point mutation, c.2304 G→T, in codon 768 of theRETproto-oncogene in a patient with medullary thyroid carcinoma-Reference-Cited by-同舟云学术

A novel germline point mutation, c.2304 G→T, in codon 768 of theRETproto-oncogene in a patient with medullary thyroid carcinoma

Published:2002-05-07 Issue:1 Volume:110 Page:85-87
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Antiñolo Guillermo,Marcos Irene,Fernández Raquel María,Romero Matilde,Borrego Salud

Funder

National Institutes of Health

Fondo de Investigacion Sanitaria

Consejeria de Salud, Comunidad Autonoma de Andalucia

Publisher

Wiley

Subject

Genetics (clinical)

Reference9 articles.

1. Recommendations for a nomenclature system for human gene mutations;Antonarakis;Hum Mutat,1998

2. Mutation of RET codon 768 is associated with the FMTC phenotype;Boccia;Clin Genet,1997

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

4. 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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