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Psychomotor development and attention problems caused by a splicing variant of CNKSR2

NIAID Data Ecosystem2026-03-12 收录

神经发育障碍

基因变异分析

数据链接：

https://www.ncbi.nlm.nih.gov/bioproject/PRJNA679981 数据链接链接失效反馈

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资源简介：

Psychomotor development and attention problems caused by a splicing variant of CNKSR2

应用场景：

创建时间：

2020-11-21

神经发育障碍

运动能力评估

To compare (1) motor proficiency of persons diagnosed in adulthood with attention deficit hyperactivity disorder (ADHD) or autism spectrum disorder (ASD) with normative values of motor proficiency, an

DataCite Commons2025-01-03 更新60

MHC.vcf.gz

免疫遗传学

基因变异分析

human MHC

DataCite Commons2024-02-21 更新50

Non-synonomous Genetic Variants of the hTP Receptor from dbSNP.

基因变异分析

蛋白质功能研究

Non-synonomous Genetic Variants of the hTP Receptor from dbSNP.

NIAID Data Ecosystem20

Table_2_Genotype–Phenotype Analysis of RPGR Variations: Reporting of 62 Chinese Families and a Literature Review.xlsx

遗传病研究

基因变异分析

PurposeRPGR is the most common cause of X-linked retinitis pigmentosa (RP), of which female carriers are also frequently affected. The aim of the current study was to explore the RPGR variation spectr

frontiersin.figshare.com2023-06-08 更新60

An Analysis of the Correlation Between Poor Short-Term Memory and Behavior in Children and Adolescents with Prader Willi Syndrome, 1996

神经发育障碍

认知行为

The purpose of the “An Analysis of the Correlation Between Poor Short-term Memory and Behavior in Children and Adolescents with Prader Willi Syndrome, 1996” was to investigate whether there were any c

DataCite Commons2023-02-28 更新40

Psychomotor development and attention problems caused by a splicing variant of CNKSR2

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