TY  - GEN
AU  - Fry,M
AU  - Loeb,L A
TI  - Human werner syndrome DNA helicase unwinds tetrahelical structures of the fragile X syndrome repeat sequence d(CGG)n
SN  - 0021-9258
PY  - 1999///0603
KW  - Base Sequence
KW  - DNA
KW  - chemistry
KW  - DNA Helicases
KW  - Fragile X Syndrome
KW  - genetics
KW  - Humans
KW  - Nucleic Acid Conformation
KW  - Trinucleotide Repeats
KW  - Werner Syndrome
KW  - enzymology
N1  - 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
UR  - https://doi.org/10.1074/jbc.274.18.12797
ER  -