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Q42752301-7B212559-E6D6-4AA7-B5DD-33110B902AA9
Q42752301-7B212559-E6D6-4AA7-B5DD-33110B902AA9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42752301-7B212559-E6D6-4AA7-B5DD-33110B902AA9
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome.
P1433
Q42752301-7B212559-E6D6-4AA7-B5DD-33110B902AA9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42752301-7B212559-E6D6-4AA7-B5DD-33110B902AA9
rank
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type
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Statement
wasDerivedFrom
9e04fbac28eb5df66c69f09da7d84ae2efa13dc8
P1433
Orphanet Journal of Rare Diseases