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Partial duplications of the ATRX gene cause the ATR-X syndrome
- Source :
- European Journal of Human Genetics. 15:1094-1097
- Publication Year :
- 2007
- Publisher :
- Springer Science and Business Media LLC, 2007.
-
Abstract
- ATR-X syndrome is a rare syndromic X-linked mental retardation disorder. We report that some of the patients suspected of ATR-X carry large intragenic duplications in the ATRX gene, leading to an absence of ATRX mRNA and of the protein. These findings underscore the need for including quantitative analyses to mutation analysis of the ATRX gene.
- Subjects :
- RNA, Messenger/genetics
Male
X-linked Nuclear Protein
DNA Mutational Analysis
Biology
medicine.disease_cause
alpha-Thalassemia
Mental Retardation, X-Linked/genetics
Gene Duplication
alpha-Thalassemia/genetics
Gene duplication
Genetics
medicine
Humans
RNA, Messenger
Gene
Genetics (clinical)
ATRX
Mutation
DNA Helicases/genetics
DNA Helicases
Infant, Newborn
Intragenic duplication
Infant
Nuclear Proteins
Syndrome
Phenotype
Nuclear Proteins/genetics
Mental Retardation, X-Linked
Mutation testing
Cancer research
Subjects
Details
- ISSN :
- 14765438 and 10184813
- Volume :
- 15
- Database :
- OpenAIRE
- Journal :
- European Journal of Human Genetics
- Accession number :
- edsair.doi.dedup.....55edcf0c1d8b81935e7cdc4a15501b06
- Full Text :
- https://doi.org/10.1038/sj.ejhg.5201878