Rett syndrome: a surprising result of mutation in MECP2
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics (clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/9/16/2365/9813817/092365.pdf
Cited by 116 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Spectrum of MECP2 mutations in Iranian Azeri Turkish Rett syndrome patients;Neurology Asia;2023-06
2. Mechanisms of robustness in gene regulatory networks involved in neural development;Frontiers in Molecular Neuroscience;2023-02-06
3. Mosaicism of common pathogenic MECP2 variants identified in two males with a clinical diagnosis of Rett syndrome;American Journal of Medical Genetics Part A;2022-08-04
4. Prevalence and Aetiopathogenesis of Intellectual Developmental Disorders;Textbook of Psychiatry for Intellectual Disability and Autism Spectrum Disorder;2022
5. Measures of attention in Rett syndrome: Internal consistency reliability.;Neuropsychology;2021-09
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