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题名

Phosphatidylinositol 4-kinase β mutations cause nonsyndromic sensorineural deafness and inner ear malformation

作者
通讯作者Jingjing Zhang; Maolian Gong
共同第一作者Yufei Feng; Sofia A. Rahman; Shuilong Wu
发表日期
2020-10-20
DOI
发表期刊
卷号47期号:10页码:618-626
收录类别
语种
英语
学校署名
其他
来源库
人工提交
引用统计
被引频次[WOS]:3
成果类型期刊论文
条目标识符http://sustech.caswiz.com/handle/2SGJ60CL/210630
专题生命科学学院_生物系
生命科学学院
前沿与交叉科学研究院
作者单位
1.Clinical Medicine Research Center, Affiliated Hospital of Inner Mongolia Medical University, Huhhot, 010050, China
2.Affiliated Hospital of Guangdong Medical University & Key Laboratory of Zebrafish Model for Development and Disease of Guangdong Medical University,Zhanjiang, 524001, China
3.Marine Medical Research Institute of Guangdong Zhanjiang, Zhanjiang, 524023, China
4.Genomic Medicine Programme, UCL Institute of Child Health and Great Ormond Street Hospital for Children, 30 Guilford Street, London, WC1N 1EH, UK
5.Max-Delbrueck-Center for Molecular Medicine (MDC), Robert-Roessle-Str.10, Berlin, 13125, Germany
6.Department of Radiology, Affiliated Hospital of Inner Mongolia Medical University, Huhhot, 010050, China
7.Affiliated People Hospital of Inner Mongolia Medical University, Huhhot, 010050, China
8.Department of Biology, Southern University of Science and Technology, Shenzhen, 518055, China
9.Guangzhou Women and Children's Medical Center, Guangzhou, 510623, China
10.Department of Radiology, Beijing Tongren Hospital, Capital Medical University, Beijing, 100730, China
11.Experimental and Clinical Research Center (ECRC), A Joint Cooperation Between the Charite Medical Faculty and the Max-Delbrueck-Center for Molecular Medicine in the Helmholtz Association (MDC), Lindenberger Weg.80, Berlin, 13125, Germany
12.Department of Paediatric Medicine Division of Endocrinology, Sidra Medical & Research Center, OPC, Doha, C6-337, Qatar
13.Medi-X Institute, SUSTec Academy for Advanced Interdisciplinary Studies, Southern University of Science and Technology, Shenzhen, 518055, China
推荐引用方式
GB/T 7714
Xiulan Su,Yufei Feng,Sofia A. Rahman,et al. Phosphatidylinositol 4-kinase β mutations cause nonsyndromic sensorineural deafness and inner ear malformation[J]. Journal of Genetics and Genomics,2020,47(10):618-626.
APA
Xiulan Su.,Yufei Feng.,Sofia A. Rahman.,Shuilong Wu.,Guoan Li.,...&Maolian Gong.(2020).Phosphatidylinositol 4-kinase β mutations cause nonsyndromic sensorineural deafness and inner ear malformation.Journal of Genetics and Genomics,47(10),618-626.
MLA
Xiulan Su,et al."Phosphatidylinositol 4-kinase β mutations cause nonsyndromic sensorineural deafness and inner ear malformation".Journal of Genetics and Genomics 47.10(2020):618-626.
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