The fragile X mental retardation syndrome protein interacts with novel homologs FXR1 and FXR2.

Fragile X Mental Retardation Syndrome is the most common form of hereditary mental retardation, and is caused by defects in the FMR1 gene. FMR1 is an RNA-binding protein and the syndrome results from lack of expression of FMR1 or expression of a mutant protein that is impaired in RNA binding. The sp...

Full beskrivning

Sparad:
Bibliografiska uppgifter
Huvudupphovsmän: Zhang, Y, O'Connor, J P, Siomi, M C, Srinivasan, S, Dutra, A, Nussbaum, R L, Dreyfuss, G
Materialtyp: Artigo
Språk:Inglês
Publicerad: 1995
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC394645/
https://ncbi.nlm.nih.gov/pubmed/7489725
Taggar: Lägg till en tagg
Inga taggar, Lägg till första taggen!

Liknande verk