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NG0193-31
NG0193-31
http://dx.doi.org/10.1038/NG0193-31
A point mutation in the FMR-1 gene associated with fragile X mental retardation.
P356
Q41579799-FB531ADE-5086-42BD-894C-0B6DE0F70792
P356
NG0193-31
http://dx.doi.org/10.1038/NG0193-31