Aspects of speech-language abilities are influenced byMECP2mutation type in girls with Rett syndrome-Reference-Cited by-同舟云学术

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Aspects of speech-language abilities are influenced byMECP2mutation type in girls with Rett syndrome

Published:2014-11-26 Issue:2 Volume:167 Page:354-362
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Urbanowicz Anna¹²,Downs Jenny¹³,Girdler Sonya⁴,Ciccone Natalie⁵,Leonard Helen¹

Affiliation:

1. Telethon Kids Institute; The University of Western Australia; Australia

2. School of Exercise and Health Sciences; Edith Cowan University; Perth WA Australia

3. School of Physiotherapy and Exercise Science; Curtin University; Perth WA Australia

4. School of Occupational Therapy and Social Work; Centre for Research into Disability and Society; Curtin University; Perth WA Australia

5. School of Psychology and Social Science; Edith Cowan University; Perth WA Australia

Funder

NHMRC

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference45 articles.

1. Predictors of scoliosis in Rett syndrome;Ager;J Child Neurol,2006

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

3. Correlation between clinical severity in patients with Rett syndrome with a p.R168X or p.T158M MECP2 mutation, and the direction and degree of skewing of X-chromosome inactivation;Archer;J Med Genet,2006

4. Using a large international sample to investigate epilepsy in Rett syndrome;Bao;Dev Med Child Neurol,2013

5. Coaching communication partners: A preliminary investigation of communication intervention during mealtime in Rett syndrome;Bartolotta;Commun Disord,2013

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3. A Severity Comparison between Italian and Israeli Rett Syndrome Cohorts;Diagnostics;2023-11-06

4. Effect of presentation rate on auditory processing in Rett syndrome: event-related potential study;Molecular Autism;2023-10-26

5. To speak may draw on epigenetic writing and reading: Unravelling the complexity of speech and language outcomes across chromatin-related neurodevelopmental disorders;Neuroscience & Biobehavioral Reviews;2023-09

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