FXR1 gene

Fragile X syndrome (FXS) is a multi-organ disease that leads to mental retardation, macro-orchidism in males and premature… (More)

FMR1 and FXR1 are RNA binding proteins interacting with the miRNA-induced silencing complex, RISC. Here we describe for the first… (More)

The loss of Fragile X mental retardation protein (FMRP) causes Fragile X syndrome, the most common inherited mental retardation… (More)

FXR1 is one of the two known homologues of FMR1. FXR1 shares a high degree of sequence homology with FMR1 and also encodes two KH… (More)

Mutations in the X-linked gene FMR1 cause fragile X syndrome, the leading cause of inherited mental retardation. Two autosomal… (More)

The clinical features of the Fragile X mental retardation syndrome are linked to the absence of the set of protein isoforms… (More)

Fragile X syndrome is the most common inherited form of mental retardation. It is caused by loss of FMR1 gene activity due to… (More)

Fragile X syndrome results from mutations in the X-linked FMR1 gene. The most common mutation is expansion and hypermethylation… (More)

Fragile X mental retardation syndrome, the most common cause of hereditary mental retardation, is directly associated with the… (More)

Fragile X Mental Retardation Syndrome is the most common form of hereditary mental retardation, and is caused by defects in the… (More)