Mutational Analysis of Methyl-CpG Binding Protein 2 (MECP2) Gene in Indian Cases of Rett Syndrome-Reference-Cited by-同舟云学术

Mutational Analysis of Methyl-CpG Binding Protein 2 (MECP2) Gene in Indian Cases of Rett Syndrome

Published:2013-02-11 Issue:2 Volume:27 Page:137-142
ISSN:0887-8013
Container-title:Journal of Clinical Laboratory Analysis
language:en
Short-container-title:J. Clin. Lab. Anal.

Author:

Das Dhanjit Kumar¹,Udani Vrajesh²,Sanghavi Daksha¹,Adhia Rashmi¹,Maitra Anurupa³

Affiliation:

1. Genetic Research Centre; National Institute for Research in Reproductive Heatlh; Mumbai; India

2. Department of Pediatric Neurology; Hinduja National Hospital and Research Centre; Mumbai; India

3. Molecular Endocrinology Department; National Institute for Research in Reproductive Heatlh; Mumbai; India

Publisher

Wiley

Subject

Microbiology (medical),Biochemistry (medical),Medical Laboratory Technology,Clinical Biochemistry,Public Health, Environmental and Occupational Health,Hematology,Immunology and Allergy

Reference17 articles.

1. Rett syndrome in Australia: A review of the epidemiology;Laourvick;J Padiatr,2006

2. Rett syndrome is caused by mutations in X-linked MeCP2, encoding methyl CpG binding protein 2;Amir;Nat Genet,1999

3. Methyl-CpG-binding protein 2 mutations in Rett syndrome;Van den Veyver;Curr Opin Genet Dev,2000

4. Methyl-CpG binding protein 2 gene (MECP2) variations in Japanese patients with Rett syndrome: Pathological mutations and polymorphisms;Fukuda;Brain Dev,2005

5. Spectrum and distribution of MECP2 mutations in 424 Rett syndrome patients: A molecular update;Philippe;Eur J Med Genet,2006

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