Genetic and clinical variations in a Norwegian sample diagnosed with Rett syndrome-Reference-Cited by-同舟云学术

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Genetic and clinical variations in a Norwegian sample diagnosed with Rett syndrome

Published:2020-08 Issue:7 Volume:42 Page:484-495
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Henriksen Mari Wold,Breck Hilde,Sejersted Yngve,Diseth Trond,von Tetzchner Stephen,Paus Benedicte,Skjeldal Ola H.

Funder

Vestre Viken Hospital Trust

Innlandet Hospital Trust

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,General Medicine,Pediatrics, Perinatology, and Child Health

Reference45 articles.

1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat Genet,1999

2. Rett syndrome: revised diagnostic criteria and nomenclature;Neul;Ann Neurol,2010

3. On a unusual brain atrophy syndrome in hyperammonemia in childhood;Rett;Wien Med Wochenschr (in German),1966

4. Rett variants: a suggested model for inclusion criteria;Hagberg;Pediatr Neurol,1994

5. Clinician's guide to genes associated with Rett-like phenotypes-Investigation of a Danish cohort and review of the literature;Schonewolf-Greulich;Clin Genet,2017

Cited by 2 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. Elav-Gal4> Mir-219 Induces Changes in Developmental Survival and Behavior in Drosophila Growth;2023

2. Technological Improvements in the Genetic Diagnosis of Rett Syndrome Spectrum Disorders;International Journal of Molecular Sciences;2021-09-26

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