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Q39125843-0EC37AF6-B5F7-4E4F-BFF0-655E3CF814AE
Q39125843-0EC37AF6-B5F7-4E4F-BFF0-655E3CF814AE
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Statement
http://www.wikidata.org/entity/statement/Q39125843-0EC37AF6-B5F7-4E4F-BFF0-655E3CF814AE
Intragenic FMR1 disease-causing variants: a significant mutational mechanism leading to Fragile-X syndrome.
P2860
Q39125843-0EC37AF6-B5F7-4E4F-BFF0-655E3CF814AE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39125843-0EC37AF6-B5F7-4E4F-BFF0-655E3CF814AE
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wasDerivedFrom
ad26f9bf1ac7ab17a6af95ce3fe0e5a1fd9d41ee
P2860
Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed males.