Molecular screening for fragile X syndrome in mentally handicapped children in Korea.

Fragile X syndrome is one of the most common forms of inherited mental retardation and is caused by the expansion of the CGG trinucleotide repeats in the FMR-1 gene. This study was aimed to facilitate the molecular screening of fragile X syndrome in Korean children with mental retardation of unknown...

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Detalles Bibliográficos
Autores principales: Kwon, S. H., Lee, K. S., Hyun, M. C., Song, K. E., Kim, J. K.
Formato: Texto
Lenguaje:English
Publicado: Korean Academy of Medical Sciences 2001
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054748/
https://www.ncbi.nlm.nih.gov/pubmed/11410685

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054748/
https://www.ncbi.nlm.nih.gov/pubmed/11410685

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