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Q41579799-2288A8DA-97FB-49F8-8CC4-A94EA3F96100
Q41579799-2288A8DA-97FB-49F8-8CC4-A94EA3F96100
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41579799-2288A8DA-97FB-49F8-8CC4-A94EA3F96100
A point mutation in the FMR-1 gene associated with fragile X mental retardation.
P2860
Q41579799-2288A8DA-97FB-49F8-8CC4-A94EA3F96100
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41579799-2288A8DA-97FB-49F8-8CC4-A94EA3F96100
rank
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type
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wasDerivedFrom
3444a23b1a81b8bd2e4efaec9f4ac19a88592cce
P2860
Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.