Title : In vitro reactivation of the FMR1 gene involved in fragile X syndrome.

Pub. Date : 1998 Jan

PMID : 9384610






1 Functional Relationships(s)
Download
Sentence
Compound Name
Protein Name
Organism
1 Most patients have a mutation in the 5" untranslated region of the FMR1 gene, consisting of the amplification of a polymorphic (CGG)nrepeat sequence, and cytogenetically express the folate-sensitive fragile site FRAXA in Xq27.3. Folic Acid fragile site, folic acid type, rare, fra(X)(q27.3) A (macroorchidism, mental retardation) Homo sapiens