A FOUR YEAR OUTCOME OF RENAL GRAFT IN A SAUDI CHILD WITH PRIMARY HYPEROXALURIA TYPE 3 SECONDARY TO A NOVEL MUTATION IN HOGA1 GENE: A CASE REPORT & REVIEW OF THE LITERATURE

Azzam Ahmad Attia; Kasem Mohammed Faheem; Almaghrabi Mohammed; Alshami Alanoud; Hamed Ammar A.

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A FOUR YEAR OUTCOME OF RENAL GRAFT IN A SAUDI CHILD WITH PRIMARY HYPEROXALURIA TYPE 3 SECONDARY TO A NOVEL MUTATION IN HOGA1 GENE: A CASE REPORT & REVIEW OF THE LITERATURE

机译：在Hoga1基因的一次新型突变中的原发性高血糖型3患儿肾移植物的四年嫁接症中的肾移植物：案例报告和文献审查

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来源
《Transplant international : 》 |2019年第s2期| 共2页
作者
Azzam Ahmad Attia; Kasem Mohammed Faheem; Almaghrabi Mohammed; Alshami Alanoud; Hamed Ammar A.;
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King Fahad Specialist Hosp Dammam Dammam Saudi Arabia;

King Fahad Specialist Hosp Dammam Dammam Saudi Arabia;

King Fahad Specialist Hosp Dammam Dammam Saudi Arabia;

King Fahad Specialist Hosp Dammam Dammam Saudi Arabia;

King Fahad Specialist Hosp Dammam Dammam Saudi Arabia;

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正文语种 eng
中图分类器官移植术 ;
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1. A FOUR YEAR OUTCOME OF RENAL GRAFT IN A SAUDI CHILD WITH PRIMARY HYPEROXALURIA TYPE 3 SECONDARY TO A NOVEL MUTATION IN HOGA1 GENE: A CASE REPORT & REVIEW OF THE LITERATURE [J] . Azzam Ahmad Attia, Kasem Mohammed Faheem, Almaghrabi Mohammed, Transplant international : . 2019 ,第S2期

机译：在Hoga1基因的一次新型突变中的原发性高血糖型3患儿肾移植物的四年嫁接症中的肾移植物：案例报告和文献审查
2. Nine novel HOGA1 gene mutations identified in primary hyperoxaluria type 3 and distinct clinical and biochemical characteristics in Chinese children [J] . Fang Xiaoliang, He Lei, Xu Guofeng, Pediatric nephrology: journal of the International Pediatric Nephrology Association . 2019 ,第10期

机译：九种新型Hoga1基因突变，鉴定在原发性高血管核尿3型中，以及中国儿童的不同临床和生化特征
3. HOGA1 Gene Mutations of Primary Hyperoxaluria Type 3 in Tunisian Patients [J] . Saoussen Mdimegh, Cécile Aquaviva‐bourdain, Asma Omezzine, Journal of clinical laboratory analysis. . 2017 ,第3期

机译：突尼斯患者原发性3型高草酸尿症HOGA1基因突变
4. UGT1A1 gene mutation and hyperthyroidism combined with hepatic failure: case report and literature review [C] . Qianyu Yan, Jingyun Fu International Conference on Biological Information and Biomedical Engineering . 2019

机译：UGT1A1基因突变和甲状腺功能亢进结合肝衰竭：案例报告和文献综述
5. U.S. primary care providers' continuing genetics education needs: A survey and literature review. [D] . Steinmark, Linda. 2009

机译：美国初级保健提供者的持续遗传学教育需求：一项调查和文献综述。
6. HOGA1 Gene Mutations of Primary Hyperoxaluria Type 3 in Tunisian Patients [O] . Saoussen Mdimegh, Cécile Aquaviva‐bourdain, Asma Omezzine, 2017

机译：突尼斯患者原发性3型高草酸尿症HOGA1基因突变
7. Mutational analysis of HOGA1 gene in Chinese pediatric patients with primary hyperoxaluria type 3 [O] . Wenying Wang, Jun Li, Ye Tian 2020

机译：初级高血管尿3型儿科患者Hoga1基因的突变分析

A FOUR YEAR OUTCOME OF RENAL GRAFT IN A SAUDI CHILD WITH PRIMARY HYPEROXALURIA TYPE 3 SECONDARY TO A NOVEL MUTATION IN HOGA1 GENE: A CASE REPORT & REVIEW OF THE LITERATURE

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