Human werner syndrome DNA helicase unwinds tetrahelical structures of the fragile X syndrome repeat sequence d(CGG)n.

Fry, M

Human werner syndrome DNA helicase unwinds tetrahelical structures of the fragile X syndrome repeat sequence d(CGG)n. [electronic resource] - The Journal of biological chemistry Apr 1999 - 12797-802 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.

0021-9258

10.1074/jbc.274.18.12797 doi


Base Sequence
DNA--chemistry
DNA Helicases--chemistry
Fragile X Syndrome--genetics
Humans
Nucleic Acid Conformation
Trinucleotide Repeats
Werner Syndrome--enzymology