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Q47943906-6B77C3CB-CF15-405F-892A-D040F3A3FA85
Q47943906-6B77C3CB-CF15-405F-892A-D040F3A3FA85
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Statement
http://www.wikidata.org/entity/statement/Q47943906-6B77C3CB-CF15-405F-892A-D040F3A3FA85
The role of CNVs in the etiology of rare autosomal recessive disorders: the example of TRAPPC9-associated intellectual disability.
P2860
Q47943906-6B77C3CB-CF15-405F-892A-D040F3A3FA85
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47943906-6B77C3CB-CF15-405F-892A-D040F3A3FA85
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Statement
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225ec89423cc144ffb34ef31a54cd027445ef4b8
P2860
Deletions of recessive disease genes: CNV contribution to carrier states and disease-causing alleles.