RET Germline Mutations Identified by Exome Sequencing in a Chinese Multiple Endocrine Neoplasia Type 2A/Familial Medullary Thyroid Carcinoma Family-Reference-Cited by-同舟云学术

RET Germline Mutations Identified by Exome Sequencing in a Chinese Multiple Endocrine Neoplasia Type 2A/Familial Medullary Thyroid Carcinoma Family

Published:2011-05-31 Issue:5 Volume:6 Page:e20353
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Qi Xiao-Ping,Ma Ju-Ming,Du Zhen-Fang,Ying Rong-Biao,Fei Jun,Jin Hang-Yang,Han Jian-Shan,Wang Jin-Quan,Chen Xiao-Ling,Chen Chun-Yue,Liu Wen-Ting,Lu Jia-Jun,Zhang Jian-Guo,Zhang Xian-Ning

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference43 articles.

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4. Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease.;G Romeo;Nature,1994

5. The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis.;C Eng;JAMA,1996

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