Mutations in the JARID1C Gene, Which Is Involved in Transcriptional Regulation and Chromatin Remodeling, Cause X-Linked Mental Retardation
- 1 February 2005
- journal article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 76 (2), 227-236
- https://doi.org/10.1086/427563
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Mutations in the FTSJ1 Gene Coding for a Novel S-Adenosylmethionine–Binding Protein Cause Nonsyndromic X-Linked Mental RetardationAmerican Journal of Human Genetics, 2004
- Foxg1 Suppresses Early Cortical Cell FateScience, 2004
- Mutations in the polyglutamine binding protein 1 gene cause X-linked mental retardationNature Genetics, 2003
- Nonsyndromic X-linked mental retardation: where are the missing mutations?Trends in Genetics, 2003
- Human PLU-1 Has Transcriptional Repression Properties and Interacts with the Developmental Transcription Factors BF-1 and PAX9Journal of Biological Chemistry, 2003
- Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsyNature Genetics, 2002
- Long mutant dystrophins and variable phenotypes: evasion of nonsense-mediated decay?Human Genetics, 2001
- The mouse Smcx gene exhibits developmental and tissue specific variation in degree of escape from X inactivationHuman Molecular Genetics, 1996
- The diagnosis and frequency of X‐linked conditions in a cohort of moderately retarded males with affected brothersAmerican Journal of Medical Genetics, 1983
- Nonspecific X‐linked mental retardation II: The frequency in British ColumbiaAmerican Journal of Medical Genetics, 1980