登录后查看消息通知
搜索
常见问题
消息
登录
首页
/
数据集
/
Additional file 2 of Novel biallelic variants in IREB2 cause an early-onset neurodegenerative disorder in a Chinese pedigree
Additional file 2 of Novel biallelic variants in IREB2 cause an early-onset neurodegenerative disorder in a Chinese pedigree
收藏
Figshare
2024-11-25 更新
2026-04-28 收录
神经退行性疾病遗传
IREB2基因研究
数据链接：
https://figshare.com/articles/dataset/Additional_file_2_of_Novel_biallelic_variants_in_IREB2_cause_an_early-onset_neurodegenerative_disorder_in_a_Chinese_pedigree/27907600
数据链接
链接失效反馈
官方服务：
问题咨询
购买咨询
在线客服
NEW
资源简介：
Supplementary Material 2
应用场景：
创建时间：
2024-11-25
相关数据集
Supplementary Material for: Association of Dopamine Beta-Hydroxylase Polymorphisms with Alzheimer’s Disease, Parkinson’s Disease and Schizophrenia: Evidence Based on Currently Available Loci
神经退行性疾病遗传
多巴胺β-羟化酶多态性
Background/Aims: The neuropathies Alzheimer’s disease (AD), Parkinson’s disease (PD), and schizophrenia (SCZ) have different pathological mechanisms but share some common neurodegenerative features, s
NIAID Data Ecosystem
8
0
Loss of function mutations in TDP-43 modifier genes.
神经退行性疾病遗传
TDP43蛋白病
Loss of function mutations in TDP-43 modifier genes.
NIAID Data Ecosystem
6
0
Negative gene correlates for APOE4- males Parietal cortex
神经退行性疾病遗传
基因表达
Negative gene correlates for APOE4- males Parietal cortex
Figshare
2019-03-13 更新
4
0
a novel splice site ALS2 variation
神经退行性疾病遗传
运动神经元基因变异
ALS2-related disorder involves retrograde degeneration of the upper motor neurons of the pyramidal tracts
NIAID Data Ecosystem
6
0
dataset related to article: "Spastic paraplegia type 46: novel and recurrent GBA2 gene variants in a compound heterozygous Italian patient with spastic ataxia phenotype"
遗传病基因诊断
神经退行性疾病遗传
Dataset contains Genetic data in VCF format of an Italian patient with spastic ataxia phenotype
Zenodo
2021-09-08 更新
4
0
© 2023-2026 上海数据发展科技有限责任公司 版权所有
沪ICP备17003045号-15
沪公网安备31010402336585号
热门搜索
社区交流群
科研交流群
商业服务
数据资源
寻源服务
数据采集
标注服务
数据产品
代理销售
数据领域
凭证登记
数据产品
介绍推广
