Exome sequencing identifies pathogenic variants in the patients with severe combined immunodeficiency

Exome sequencing identifies pathogenic variants in the patients with severe combined immunodeficiency

碩士 === 國立成功大學 === 臨床醫學研究所 === 103

Bibliographic Details
Main Authors:	Cheng-YuLiao, 廖正宇
Other Authors:	Peng-Chieh Chen
Format:	Others
Language:	en_US
Published:	2015
Online Access:	http://ndltd.ncl.edu.tw/handle/44uakj

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