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Partial protoporphyrinogen oxidase (PPOX) gene deletions, due to different Alu-mediated mechanisms, identified by MLPA analysis in patients with variegate porphyria

机译：局部原卟啉原氧化酶（<它> ppOX ）基因缺失，由于不同<它>铝介导的机制，在患者斓卟啉赞许通过mLpa分析

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Barbaro Michela; Kotajärvi Maire; Harper Pauline; Floderus Ylva;
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年度 2013
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1. Partial protoporphyrinogen oxidase (PPOX) gene deletions, due to different Alu-mediated mechanisms, identified by MLPA analysis in patients with variegate porphyria [J] . Michela Barbaro, Maire Kotaj?rvi, Pauline Harper, Orphanet journal of rare diseases . 2013,第2期

机译：通过不同的Alu介导的机制，部分原卟啉原氧化酶（PPOX）基因缺失，通过MLPA分析在杂色卟啉症患者中鉴定
2. Identification of a recurrent mutation in the protoporphyrinogen oxidase gene in Swiss patients with variegate porphyria: clinical and genetic implications. [J] . Van Tuyll Van Serooskerke AM, Schneider Yin X, Schimmel RJ, Cellular and molecular biology . 2009,第2期

机译：瑞士斑驳性卟啉症患者原卟啉原氧化酶基因复发突变的鉴定：临床和遗传意义。
3. Novel heterozygous mutation of protoporphyrinogen oxidase gene in a Chinese patient with variegate porphyria [J] . Zhou Shengru, Zhao Xiaoqing, Kang Hongyan, The Journal of dermatology . 2017,第12期

机译：具有杂色卟啉卟啉患者在中国患者中的新型杂合酶突变
4. Understanding the Mechanism of Drug Resistance Due to a Codon Deletion in Protoporphyrinogen Oxidase through Computational Modeling [C] . Ge-Fei Hao, Xiao-Lei Zhu, Feng-Qin Ji, ICMSI;International conference of molecular simulations and applied informatics technologies . 2010

机译：通过计算模型了解原卟啉原氧化酶密码子缺失导致的耐药机制。
5. Protoporphyrinogen oxidase (PPOX) targeted gene silencing based photodynamic therapy (PDT) in combination with photofrin-PDT. [D] . Ganesan, Srikanth. 2007

机译：原卟啉原氧化酶（PPOX）靶向基因沉默的光动力疗法（PDT）与photofrin-PDT组合。
6. Partial protoporphyrinogen oxidase (PPOX) gene deletions due to different Alu-mediated mechanisms identified by MLPA analysis in patients with variegate porphyria [O] . Michela Barbaro, Maire Kotajärvi, Pauline Harper, 2013

机译：通过不同的Alu介导的机制部分原卟啉原氧化酶（PPOX）基因缺失通过MLPA分析在杂色性卟啉症患者中鉴定
7. Partial protoporphyrinogen oxidase (PPOX) gene deletions, due to different Alu-mediated mechanisms, identified by MLPA analysis in patients with variegate porphyria [O] . Barbaro Michela, Kotajärvi Maire, Harper Pauline, 2013

机译：通过不同的 Alu 介导的机制，部分原卟啉原氧化酶（ PPOX ）基因缺失，通过MLPA分析鉴定为斑状卟啉症患者

Partial protoporphyrinogen oxidase (PPOX) gene deletions, due to different Alu-mediated mechanisms, identified by MLPA analysis in patients with variegate porphyria

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