Enrichment of mutations in chromatin regulators in people with Rett syndrome lacking mutations in MECP2-Reference-Cited by-同舟云学术

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Enrichment of mutations in chromatin regulators in people with Rett syndrome lacking mutations in MECP2

Published:2017-01 Issue:1 Volume:19 Page:13-19
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Sajan Samin A.,Jhangiani Shalini N.,Muzny Donna M.,Gibbs Richard A.,Lupski James R.,Glaze Daniel G.,Kaufmann Walter E.,Skinner Steven A.,Annese Fran,Friez Michael J.,Lane Jane,Percy Alan K.,Neul Jeffrey L.

Publisher

Elsevier BV

Subject

Genetics (clinical)

Link

http://www.nature.com/articles/gim201642.pdf

Reference41 articles.

Cited by 61 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

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3. A Narrative Review on the Use of Eye-Tracking in Rett Syndrome: Implications for Diagnosis and Treatment;OBM Genetics;2024-07-05

4. Preliminary Study on Clinical Characteristics and Pathogenesis of IQSEC2 Mutations Patients;Pharmacogenomics and Personalized Medicine;2024-05

5. Comprehensive Transcriptomic Investigation of Rett Syndrome Reveals Increasing Complexity Trends from Induced Pluripotent Stem Cells to Neurons with Implications for Enriched Pathways;ACS Omega;2023-11-08

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