نتائج البحث - Wei‐Xia Lin

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  1. 1
    Molecular diagnosis of pediatric patients with citrin deficiency in China: SLC25A13 mutation spectrum and the geographic distribution

    Molecular diagnosis of pediatric patients with citrin deficiency in China: SLC25A13 mutation spectrum and the geographic distribution حسب Wei‐Xia Lin, Han-Shi Zeng, Zhan‐Hui Zhang, Man Mao, Qi-Qi Zheng, Shutao Zhao, Ying Cheng, Fengping Chen, Wangrong Wen, Yuan‐Zong Song

    منشور في 2016
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    Artigo
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    محفوظ في:
  2. 2
    SLC25A13 Gene Analysis in Citrin Deficiency: Sixteen Novel Mutations in East Asian Patients, and the Mutation Distribution in a Large Pediatric Cohort in China

    SLC25A13 Gene Analysis in Citrin Deficiency: Sixteen Novel Mutations in East Asian Patients, and the Mutation Distribution in a Large Pediatric Cohort in China حسب Yuan‐Zong Song, Zhan‐Hui Zhang, Wei‐Xia Lin, Xin-Jing Zhao, Mei Deng, Yanli Ma, Guo Li, Fengping Chen, Xiaoling Long, Xiangling He, Yoshihide Sunada, Shun Soneda, Akiko Nakatomi, Sumito Dateki, Lock Hock Ngu, Keiko Kobayashi, Takeyori Saheki

    منشور في 2013
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    Artigo
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