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Q37138653-0407EB8F-5D0E-43C2-9EA0-0BA1882116EF
Q37138653-0407EB8F-5D0E-43C2-9EA0-0BA1882116EF
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Statement
http://www.wikidata.org/entity/statement/Q37138653-0407EB8F-5D0E-43C2-9EA0-0BA1882116EF
NAHR-mediated copy-number variants in a clinical population: mechanistic insights into both genomic disorders and Mendelizing traits.
P2860
Q37138653-0407EB8F-5D0E-43C2-9EA0-0BA1882116EF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37138653-0407EB8F-5D0E-43C2-9EA0-0BA1882116EF
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Statement
wasDerivedFrom
c3b6916df01c8f1719bcb21624fd66b5d055e9bd
P2860
Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome.