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A Novel Variant in Non-coding Region of GJB1 Is Associated With X-Linked Charcot-Marie-Tooth Disease Type 1 and Transient CNS Symptoms
期刊论文
FRONTIERS IN NEUROLOGY, 2019, 卷号: 10
作者:
Luo, Si
;
Jin, Hui
;
Chen, Jiajun
;
Zhang, Lei
收藏
  |  
浏览/下载:6/0
  |  
提交时间:2019/12/05
Charcot-Marie-Tooth disease
GJB1
central nervous system manifestations
variant
pedigree
Complex ATP7B mutation patterns in Wilson disease and evaluation of a yeast model for functional analysis of variants
期刊论文
HUMAN MUTATION, 2019, 卷号: 40, 期号: 5
作者:
Lv, Tingxia
;
Li, Xiaojin
;
Zhang, Wei
;
Zhou, Donghu
;
Xu, Anjian
收藏
  |  
浏览/下载:38/0
  |  
提交时间:2019/12/05
ATP7B mutation pattern
Functional consequence
Pedigree analysis
Wilson disease
Yeast model
SCN4A p.R675Q Mutation Leading to Normokalemic Periodic Paralysis: A Family Report and Literature Review
期刊论文
FRONTIERS IN NEUROLOGY, 2019, 卷号: 10
作者:
Shi, Jiejing
;
Qu, Qianqian
;
Liu, Haiyan
;
Cui, Wenhao
;
Zhang, Yan
收藏
  |  
浏览/下载:22/0
  |  
提交时间:2019/12/05
normokalemic periodic paralysis
SCN4A mutation
muscle imaging
muscle biopsy
pedigree
Characteristics and Follow-Up of 13 pedigrees with Gitelman syndrome
期刊论文
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 2019, 卷号: 42, 期号: 6, 页码: 653-665
作者:
Zhong, F.
;
Ying, H.
;
Jia, W.
;
Zhou, X.
;
Zhang, H.
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/11
Gitelman syndrome
Pedigree
Solute carrier family 12
member 3
(SLC12A3)
Genotype
Phenotype
Follow-up
Cervical Spinal Involvement in a Chinese Pedigree With Pontine Autosomal Dominant Microangiopathy and Leukoencephalopathy Caused by a 3 ' Untranslated Region Mutation of COL4A1 Gene
期刊论文
STROKE, 2019, 卷号: 50, 期号: 9, 页码: 2307-2313
作者:
Zhao, Yu-Ying
;
Duan, Ruo-Nan
;
Ji, Lin
;
Liu, Qi-Ji
;
Yan, Chuan-Zhu
收藏
  |  
浏览/下载:17/0
  |  
提交时间:2019/12/11
brain
cerebral small vessel disease
collagen
leukoencephalopathies
magnetic resonance imaging
mutation
pedigree
Sarcomere variants in arrhythmogenic cardiomyopathy: Pathogenic factor or bystander?
期刊论文
2019, 卷号: 687, 页码: 82-89
作者:
Chen, Kai
;
Rao, Man
;
Guo, Guangran
;
Chen, Xiao
;
Chen, Liang
收藏
  |  
浏览/下载:6/0
  |  
提交时间:2020/01/03
Arrhythmogenic cardiomyopathy
Genetics
Sarcomere variants
Arrhythmia
Pedigree analysis
Novel mutation in FTHL17 gene in pedigree with 46,XY pure gonadal dysgenesis
期刊论文
2019, 卷号: 111, 期号: 6, 页码: 1226-+
作者:
Tang, Ruiyi
;
Liu, Xiao
;
Pan, Lingya
;
Chen, Rong
收藏
  |  
浏览/下载:5/0
  |  
提交时间:2020/01/03
46
XY pure gonadal dysgenesis
family pedigree
ferritin heavy chain-like 17
gonadal tumor
whole-genome sequencing
Algorithms for Pedigree Comparison
期刊论文
IEEE/ACM Transactions on Computational Biology and Bioinformatics, 2018, 卷号: 15, 期号: 2, 页码: 422-431
作者:
Chen, Zhi-Zhong*
;
Feng, Qilong
;
Shen, Chao
;
Wang, Jianxin
;
Wang, Lusheng
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/03
Pedigree
fixed-parameter algorithm
NP-hardness
Investigation of inflammatory bowel disease risk factors in 4 families in central China
期刊论文
EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2018, 卷号: 15, 期号: 2
作者:
Xu, Shufang
;
Zou, Hui
;
Zhang, Heng
;
Zhu, Siying
;
Zhou, Rui
收藏
  |  
浏览/下载:10/0
  |  
提交时间:2019/12/05
pedigree analysis
inflammatory bowel disease
Crohn's disease
ulcerative colitis
genetic susceptibility
genetic heterogeneity
Characteristics and Follow-Up of 13 pedigrees with Gitelman syndrome
期刊论文
Journal of Endocrinological Investigation, 2018
作者:
Zhong F.
;
Ying H.
;
Jia W.
;
Zhou X.
;
Zhang H.
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/11
Follow-up
Genotype
Gitelman syndrome
Pedigree
Phenotype
Solute carrier family 12, member 3 (SLC12A3)
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