Phenotypic variability in Rett syndrome associated with FOXG1 mutations in females-Reference-Cited by-同舟云学术

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Phenotypic variability in Rett syndrome associated with FOXG1 mutations in females

Published:2009-06-29 Issue:1 Volume:47 Page:59-65
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Philippe C.,Amsallem D.,Francannet C.,Lambert L.,Saunier A.,Verneau F.,Jonveaux P.

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Cited by 79 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. Menin Deficiency Induces Autism‐Like Behaviors by Regulating Foxg1 Transcription and Participates in Foxg1‐Related Encephalopathy;Advanced Science;2024-04-06

2. Genomic analysis in Chilean patients with suspected Rett syndrome: keep a broad differential diagnosis;Frontiers in Genetics;2024-03-18

3. FOXG1 variants can be associated with milder phenotypes than congenital Rett syndrome with unassisted walking and language development;American Journal of Medical Genetics Part B: Neuropsychiatric Genetics;2024-03-08

4. Role of MeCP2 in oligodendrocyte lineage cells in Rett syndrome: review and inference;Ageing and Neurodegenerative Diseases;2023-07-19

5. Expanding genotype–phenotype correlations in FOXG1 syndrome: results from a patient registry;Orphanet Journal of Rare Diseases;2023-06-12

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