Scrutinizing the molecular, biochemical, and cytogenetic attributes in subjects with Rett syndrome (RTT) and their mothers-Reference-Cited by-同舟云学术

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Scrutinizing the molecular, biochemical, and cytogenetic attributes in subjects with Rett syndrome (RTT) and their mothers

Published:2020-10 Issue: Volume:111 Page:107277
ISSN:1525-5050
Container-title:Epilepsy & Behavior
language:en
Short-container-title:Epilepsy & Behavior

Author:

Meyyazhagan Arun,Balasubramanian Balamuralikrishnan,Kathannan Sankar,Alagamuthu Karthick Kumar,Easwaran Murugesh,Shanmugam Sureshkumar,Pappusamy Manikantan,Bhotla Haripriya Kuchi,Mustaqahamed Shafiahammedkhan,Arumugam Vijaya Anand,Kaul Tanushri,Keshavarao Sasikala

Publisher

Elsevier BV

Subject

Behavioral Neuroscience,Clinical Neurology,Neurology

Reference45 articles.

1. Recent progress in Rett syndrome and MeCP2 dysfunction: assessment of potential treatment options;Chapleau;Future Neurol,2013

2. MECP2 variation in Rett syndrome—an overview of current coverage of genetic and phenotype data within existing databases;Townend;Hum Mutat,2018

3. Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes;Amir;Ann Neurol,2000

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

5. Rett syndrome–biological pathways leading from MECP2 to disorder phenotypes;Ehrhart;Orphanet J Rare Dis,2016

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