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Q33399905-12FD2D6A-C160-4F49-86A4-86FE9D3C6BCE
Q33399905-12FD2D6A-C160-4F49-86A4-86FE9D3C6BCE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33399905-12FD2D6A-C160-4F49-86A4-86FE9D3C6BCE
Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome.
P2860
Q33399905-12FD2D6A-C160-4F49-86A4-86FE9D3C6BCE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33399905-12FD2D6A-C160-4F49-86A4-86FE9D3C6BCE
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wasDerivedFrom
0cc63ffb9c896eaaae36f7755af2e4fe78218071
P2860
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.