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Q41919819-7D713825-5DE3-44A3-9431-DAECE892D872
Q41919819-7D713825-5DE3-44A3-9431-DAECE892D872
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http://www.wikidata.org/entity/statement/Q41919819-7D713825-5DE3-44A3-9431-DAECE892D872
Exonic microdeletions in the X-linked PQBP1 gene in mentally retarded patients: a pathogenic mutation and in-frame deletions of uncertain effect.
P2860
Q41919819-7D713825-5DE3-44A3-9431-DAECE892D872
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41919819-7D713825-5DE3-44A3-9431-DAECE892D872
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wasDerivedFrom
e693a00b6ca65e11d15749c5f5f5beff4ad868a6
P2860
Novel truncating mutations in the polyglutamine tract binding protein 1 gene (PQBP1) cause Renpenning syndrome and X-linked mental retardation in another family with microcephaly