KDM5C mutational screening among males with intellectual disability suggestive of X-Linked inheritance and review of the literature-Reference-Cited by-同舟云学术

KDM5C mutational screening among males with intellectual disability suggestive of X-Linked inheritance and review of the literature

Published:2014-03 Issue:4 Volume:57 Page:138-144
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Gonçalves Thainá Fernandez,Gonçalves Andressa Pereira,Fintelman Rodrigues Natalia,dos Santos Jussara Mendonça,Pimentel Márcia Mattos Gonçalves,Santos-Rebouças Cíntia Barros

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference38 articles.

1. Mutations in JARID1C are associated with X-linked mental retardation, short stature and hyperreflexia;Abidi;J Med Genet,2008

2. A novel mutation in JARID1C/SMCX in a patient with autism spectrum disorder (ASD);Adegbola;Am J Med Genet A,2008

3. The influence of expanded unmethylated alleles for FRAXA/FRAXE loci in the intellectual performance among Brazilian mentally impaired males;Barros Santos;Int J Mol Med,2003

4. Low significance of MECP2 mutations as a cause of mental retardation in Brazilian males;Campos;Brain Dev,2007

5. High frequency of nonrecurrent MECP2 duplications among Brazilian males with mental retardation;Campos;J Mol Neurosci,2010

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