首页> 外文OA文献 >Bilirubin-uridine diphosphate glucuronosyltransferase (UGT1A1) gene mutations among newborn babies in the Malay population in Kelantan with hyperbilirubinaemia RJ276. S961 2005 f rb.

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Bilirubin-uridine diphosphate glucuronosyltransferase (UGT1A1) gene mutations among newborn babies in the Malay population in Kelantan with hyperbilirubinaemia RJ276. S961 2005 f rb.

机译：吉兰丹州马来人群高胆红素血症的新生婴儿中胆红素-尿苷二磷酸葡萄糖醛酸转移酶（UGT1A1）基因突变RJ276。 S961 2005 frb。

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Sindrom Gilbert berpunca daripada keabnormalan pada gen uridine diphosphate-glucuronosyltransferase 1A1 (UGT1A1) yang disebabkan oleh mutasi.ududGilbert syndrome is caused by defects in the uridine diphosphateglucuronosyltransferase 1A1 (UGT1A1) gene.ud

机译：吉尔伯特综合症是由突变引起的尿苷二磷酸-葡糖醛酸糖基转移酶1A1（UGT1A1）基因异常引起的。

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Yusoff Surini;
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1. Crigler-Najjar syndrome type II in a Chinese boy resulting from three mutations in the bilirubin uridine 5′-diphosphate-glucuronosyltransferase (UGT1A1) gene and a family genetic analysis [J] . Bixia Zheng, Guorui Hu, Jin Yu, BMC Pediatrics . 2014,第1期

机译：一名中国男孩的Crigler-Najjar综合征II型，归因于胆红素尿苷5'-二磷酸-葡萄糖尿苷转移酶（UGT1A1）基因的三个突变和家庭遗传分析
2. Frequency of G71E and Detection of a Novel Mutation in Exon 1 of the UGT1A1 Gene In a Malay Population [J] . Maamor NH, Yusoff S, Alwi Zilfalil B, International medical journal: IMJ . 2012,第2期

机译：马来族群中G71E的频率和UGT1A1基因外显子1中新突变的检测
3. Interaction of coding region mutations and the Gilbert-type promoter abnormality of the UGT1A1 gene causes moderate degrees of unconjugated hyperbilirubinaemia and may lead to neonatal kernicterus. [J] . Kadakol A, Sappal BS, Ghosh SS, Journal of Medical Genetics . 2001,第4期

机译：UGT1A1基因的编码区突变和吉尔伯特型启动子异常的相互作用导致中等程度的未结合的高胆红素血症，并可能导致新生儿角膜炎。
4. Crigler-Najjar syndrome type II in a Chinese boy resulting from three mutations in the bilirubin uridine 5′-diphosphate-glucuronosyltransferase (UGT1A1) gene and a family genetic analysis [O] . Bixia Zheng, Guorui Hu, Jin Yu, 2014

机译：一名中国男孩的Crigler-Najjar综合征II型归因于胆红素尿苷5-二磷酸-葡萄糖醛酸转移酶（UGT1A1）基因的三个突变和家庭遗传分析
5. Bilirubin-uridine diphosphate glucuronosyltransferase (UGT1A1) gene mutations among newborn babies in the Malay population in Kelantan with hyperbilirubinaemia RJ276. S961 2005 f rb. [O] . Yusoff Surini 2005

机译：吉兰丹州马来人群高胆红素血症的新生婴儿中胆红素-尿苷二磷酸葡萄糖醛酸转移酶（UGT1A1）基因突变RJ276。 S961 2005 frb。

Bilirubin-uridine diphosphate glucuronosyltransferase (UGT1A1) gene mutations among newborn babies in the Malay population in Kelantan with hyperbilirubinaemia RJ276. S961 2005 f rb.

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