个人科研网厅 | | 帮助
高级检索
当前位置： 首页 > 详情页

Novel NPHS1 gene mutations in a Chinese family with congenital nephrotic syndrome

| 认领 | 导出 | |

文献详情

资源类型：
WOS体系：
Pubmed体系：

收录情况： ◇ SCIE

作者：
Yang, Fengjie[1] * ; Chen, Yaxian[1] ; Zhang, Yu[1] ; Qiu, Liru[1] ; Chen, Yu[1] ; Zhou, Jianhua[1] ;
单位： [1]Huazhong Univ Sci & Technol, Dept Pediat, Tongji Hosp, Tongji Med Coll, Wuhan 430030, Hubei, Peoples R China
出处：
DOI： 10.1007/s12041-015-0598-6
ISSN：

关键词： congenital nephrotic syndrome of Finnish type compound heterozygous mutations NPHS1 gene Chinese family

基金：
National Natural Science Foundation of China [81070557]; Natural Science Foundation of Hubei province [2011CDB553]
语种：
外文
被引次数：
WOS：
PubmedID：
中科院(CAS)分区：
出版当年[2015]版：
大类 | 4 区 生物
小类 | 4 区 遗传学
最新[2025]版：
大类 | 4 区 生物学
小类 | 4 区 遗传学
JCR分区：
出版当年[2014]版：
Q4 GENETICS & HEREDITY
最新[2024]版：
Q4 GENETICS & HEREDITY

影响因子： 最新[2024版] 最新五年平均 出版当年[2014版] 出版当年五年平均 出版前一年[2013版] 出版后一年[2015版]

第一作者：
第一作者单位： [1]Huazhong Univ Sci & Technol, Dept Pediat, Tongji Hosp, Tongji Med Coll, Wuhan 430030, Hubei, Peoples R China
通讯作者：
推荐引用方式(GB/T 7714)：
Yang Fengjie,Chen Yaxian,Zhang Yu,et al.Novel NPHS1 gene mutations in a Chinese family with congenital nephrotic syndrome[J].JOURNAL OF GENETICS.2016,95(1):161-166.doi:10.1007/s12041-015-0598-6.
APA：
Yang, Fengjie,Chen, Yaxian,Zhang, Yu,Qiu, Liru,Chen, Yu&Zhou, Jianhua.(2016).Novel NPHS1 gene mutations in a Chinese family with congenital nephrotic syndrome.JOURNAL OF GENETICS,95,(1)
MLA：
Yang, Fengjie,et al."Novel NPHS1 gene mutations in a Chinese family with congenital nephrotic syndrome".JOURNAL OF GENETICS 95..1(2016):161-166

相关文献

[1]Identification of compound heterozygous mutations in GNPTG in three siblings of a Chinese family with mucolipidosis type III gamma [2]芬兰型先天性肾病综合征1例家系基因分析及文献复习 [3]Case report: Autosomal recessive type 3 Stickler syndrome caused by compound heterozygous mutations in COL11A2 [4]Compound heterozygous ZP1 mutations cause empty follicle syndrome in infertile sisters [5]Novel compound heterozygous mutations in WEE2 causes female infertility and fertilization failure [6]The Potential Effect of Nav1.8 in Autism Spectrum Disorder: Evidence From a Congenital Case With Compound Heterozygous SCN10A Mutations [7]Novel compound heterozygous mutations in the SPTA1 gene, causing hereditary spherocytosis in a neonate with Coombs-negative hemolytic jaundice [8]Novel compound heterozygous mutations in DNAH1 cause primary infertility in Han Chinese males with multiple morphological abnormalities of the sperm flagella [9]Mutation analysis of a Chinese family with oculocutaneous albinism [10]The same heterozygous Col4A4 mutation triggered different renal pathological changes in Chinese family members

资源点击量：622 今日访问量：0 总访问量：452 更新日期：2025-07-01 建议使用谷歌、火狐浏览器 常见问题

版权所有：重庆聚合科技有限公司 渝ICP备12007440号-3 地址：重庆市两江新区泰山大道西段8号坤恩国际商务中心16层（401121）