A new regulatory pathway for fragile X syndrome?

One out of every 4,500 males suffers cognitive impairment due to alterations in the fragile X gene. The gene has a complicated biology, and it may have just gotten a bit more complex. The fragile X gene product in flies could play a role in regulation by small RNA molecules.

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Veröffentlicht in:Nature medicine 2002-11, Vol.8 (11), p.1204-1205
Hauptverfasser: Hansen, R. Scott, Laird, Charles D
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creator Hansen, R. Scott
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description One out of every 4,500 males suffers cognitive impairment due to alterations in the fragile X gene. The gene has a complicated biology, and it may have just gotten a bit more complex. The fragile X gene product in flies could play a role in regulation by small RNA molecules.
doi_str_mv 10.1038/nm1102-1204
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subjects Animals
Drosophila - genetics
Fragile X Mental Retardation Protein
Fragile X syndrome
Fragile X Syndrome - genetics
Genetic aspects
Health aspects
Humans
Male
Methylation
Nerve Tissue Proteins - genetics
Nerve Tissue Proteins - physiology
Risk factors
RNA - physiology
RNA-Binding Proteins
title A new regulatory pathway for fragile X syndrome?
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