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Q41925091-42950C01-349E-491D-AD2C-DAD5CE2A3705
Q41925091-42950C01-349E-491D-AD2C-DAD5CE2A3705
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41925091-42950C01-349E-491D-AD2C-DAD5CE2A3705
Autosomal recessive mutations in THOC6 cause intellectual disability: syndrome delineation requiring forward and reverse phenotyping.
P2860
Q41925091-42950C01-349E-491D-AD2C-DAD5CE2A3705
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41925091-42950C01-349E-491D-AD2C-DAD5CE2A3705
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wasDerivedFrom
7aafc698b340b6b1f233718dcf45f366e5a4d3a6
P2860
DECIPHER: database for the interpretation of phenotype-linked plausibly pathogenic sequence and copy-number variation